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Previous release (v1)
2026-10-05 18:56:45, GGRNA.v2 : RefSeq release 233 (Jan, 2026)
LOCUS NR_029413 2024 bp RNA linear PRI 06-AUG-2023
DEFINITION Homo sapiens MFNG O-fucosylpeptide
3-beta-N-acetylglucosaminyltransferase (MFNG), transcript variant
3, non-coding RNA.
ACCESSION NR_029413 XM_005261607
VERSION NR_029413.2
KEYWORDS RefSeq.
SOURCE Homo sapiens (human)
ORGANISM Homo sapiens
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
Catarrhini; Hominidae; Homo.
REFERENCE 1 (bases 1 to 2024)
AUTHORS Gao Y, Luo L, Qu Y and Zhou Q.
TITLE MFNG is an independent prognostic marker for osteosarcoma
JOURNAL Eur J Med Res 28 (1), 256 (2023)
PUBMED 37496053
REMARK GeneRIF: MFNG is an independent prognostic marker for osteosarcoma.
Publication Status: Online-Only
REFERENCE 2 (bases 1 to 2024)
AUTHORS Cheng WK, Kaur G, Sjoberg E, Frodin M, Egevad L, Harmenberg U, Li
JL and Oon CE.
TITLE Nuclear and stromal expression of Manic fringe in renal cell
carcinoma
JOURNAL Exp Mol Pathol 122, 104667 (2021)
PUBMED 34371013
REMARK GeneRIF: Nuclear and stromal expression of Manic fringe in renal
cell carcinoma.
REFERENCE 3 (bases 1 to 2024)
AUTHORS Lopez-Arribillaga E, Rodilla V, Colomer C, Vert A, Shelton A, Cheng
JH, Yan B, Gonzalez-Perez A, Junttila MR, Iglesias M, Torres F,
Albanell J, Villanueva A, Bigas A, Siebel CW and Espinosa L.
TITLE Manic Fringe deficiency imposes Jagged1 addiction to intestinal
tumor cells
JOURNAL Nat Commun 9 (1), 2992 (2018)
PUBMED 30065304
REMARK GeneRIF: MFNG imposes a negative correlation between Jag1 and
Notch, being high Jag1 in the absence of MFNG predictive of poor
prognosis.
Publication Status: Online-Only
REFERENCE 4 (bases 1 to 2024)
AUTHORS Zhang S, Chung WC, Wu G, Egan SE, Miele L and Xu K.
TITLE Manic fringe promotes a claudin-low breast cancer phenotype through
notch-mediated PIK3CG induction
JOURNAL Cancer Res 75 (10), 1936-1943 (2015)
PUBMED 25808869
REMARK GeneRIF: Mfng is an oncogene acting through Notch-mediated
induction of Pik3cg.
REFERENCE 5 (bases 1 to 2024)
AUTHORS Davila S, Froeling FE, Tan A, Bonnard C, Boland GJ, Snippe H,
Hibberd ML and Seielstad M.
TITLE New genetic associations detected in a host response study to
hepatitis B vaccine
JOURNAL Genes Immun 11 (3), 232-238 (2010)
PUBMED 20237496
REMARK GeneRIF: Observational study of gene-disease association. (HuGE
Navigator)
REFERENCE 6 (bases 1 to 2024)
AUTHORS Moran JL, Johnston SH, Rauskolb C, Bhalerao J, Bowcock AM and Vogt
TF.
TITLE Genomic structure, mapping, and expression analysis of the
mammalian Lunatic, Manic, and Radical fringe genes
JOURNAL Mamm Genome 10 (6), 535-541 (1999)
PUBMED 10341080
REFERENCE 7 (bases 1 to 2024)
AUTHORS Van Tine BA, Knops J, Shaw GM and May WA.
TITLE Assignment of human MFNG, manic fringe Drosophila homolog, to
22q13.1 using tyramide fluorescence in situ hybridization (T-FISH)
JOURNAL Cytogenet Cell Genet 87 (1-2), 132-133 (1999)
PUBMED 10640833
REFERENCE 8 (bases 1 to 2024)
AUTHORS Egan S, Herbrick JA, Tsui LC, Cohen B, Flock G, Beatty B and
Scherer SW.
TITLE Mapping of the human Lunatic Fringe (LFNG) gene to 7p22 and Manic
Fringe (MFNG) to 22q12
JOURNAL Genomics 54 (3), 576-577 (1998)
PUBMED 9878264
REFERENCE 9 (bases 1 to 2024)
AUTHORS Cohen B, Bashirullah A, Dagnino L, Campbell C, Fisher WW, Leow CC,
Whiting E, Ryan D, Zinyk D, Boulianne G, Hui CC, Gallie B, Phillips
RA, Lipshitz HD and Egan SE.
TITLE Fringe boundaries coincide with Notch-dependent patterning centres
in mammals and alter Notch-dependent development in Drosophila
JOURNAL Nat Genet 16 (3), 283-288 (1997)
PUBMED 9207795
REFERENCE 10 (bases 1 to 2024)
AUTHORS Johnston SH, Rauskolb C, Wilson R, Prabhakaran B, Irvine KD and
Vogt TF.
TITLE A family of mammalian Fringe genes implicated in boundary
determination and the Notch pathway
JOURNAL Development 124 (11), 2245-2254 (1997)
PUBMED 9187150
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from DA815501.1, AK316555.1,
BC094814.1 and AI363008.1.
On Jul 11, 2019 this sequence version replaced NR_029413.1.
Summary: This gene is a member of the glycosyltransferase 31 gene
family. Members of this gene family, which also includes the LFNG
(GeneID: 3955) and RFNG (GeneID: 5986) genes, encode evolutionarily
conserved glycosyltransferases that act in the Notch signaling
pathway to define boundaries during embryonic development. While
their genomic structure is distinct from other
glycosyltransferases, these proteins have a fucose-specific
beta-1,3-N-acetylglucosaminyltransferase activity that leads to
elongation of O-linked fucose residues on Notch, which alters Notch
signaling. The protein encoded by this gene may control Notch
signaling in claudin-low breast cancer. [provided by RefSeq, May
2018].
Transcript Variant: This variant (3) lacks an alternate internal
exon, compared to variant 1. This variant is represented as
non-coding because the use of the 5'-most supported translational
start codon, as used in variant 1, renders the transcript a
candidate for nonsense-mediated mRNA decay (NMD).
Publication Note: This RefSeq record includes a subset of the
publications that are available for this gene. Please see the Gene
record to access additional publications.
##Evidence-Data-START##
Transcript exon combination :: SRR1803611.23018.1,
SRR1163655.48752.1 [ECO:0000332]
RNAseq introns :: mixed sample support SAMEA1965299,
SAMEA1966682 [ECO:0006172]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-3 DA815501.1 57-59
4-1174 AK316555.1 1-1171
1175-2019 BC094814.1 1241-2085
2020-2024 AI363008.1 1-5 c
FEATURES Location/Qualifiers
source 1..2024
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="22"
/map="22q13.1"
gene 1..2024
/gene="MFNG"
/note="MFNG O-fucosylpeptide
3-beta-N-acetylglucosaminyltransferase"
/db_xref="GeneID:4242"
/db_xref="HGNC:HGNC:7038"
/db_xref="MIM:602577"
misc_RNA 1..2024
/gene="MFNG"
/product="MFNG O-fucosylpeptide
3-beta-N-acetylglucosaminyltransferase, transcript variant
3"
/db_xref="GeneID:4242"
/db_xref="HGNC:HGNC:7038"
/db_xref="MIM:602577"
exon 1..462
/gene="MFNG"
/inference="alignment:Splign:2.1.0"
variation 3
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789369"
variation 4
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:1025231980"
variation 6
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1294633243"
variation 7
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1922560232"
variation 8..13
/gene="MFNG"
/replace="gga"
/replace="ggagga"
/db_xref="dbSNP:2517789350"
variation 10
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1922560120"
variation 12
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1315962034"
variation 14
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1225332419"
variation 15
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1263821524"
variation 16
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1196066277"
variation 17
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789341"
variation 18
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789340"
variation 19
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1009537029"
variation 20..26
/gene="MFNG"
/replace="g"
/replace="gcggtcg"
/db_xref="dbSNP:2517789320"
variation 20
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:370756546"
variation 21
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922559000"
variation 22
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1053851345"
variation 23
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789329"
variation 24
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922558658"
variation 25
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1486376672"
variation 26..37
/gene="MFNG"
/replace="g"
/replace="gagatcgtgctg"
/db_xref="dbSNP:2517789296"
variation 26..29
/gene="MFNG"
/replace="gaga"
/replace="gagaga"
/db_xref="dbSNP:2517789313"
variation 26
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:535073824"
variation 29
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789308"
variation 31
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1186266754"
variation 32
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1001338338"
variation 34
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1177873222"
variation 35
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517789297"
variation 37
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145743157"
variation 38
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:988224086"
variation 39..40
/gene="MFNG"
/replace=""
/replace="gtatcattaaaaa"
/db_xref="dbSNP:2517789287"
variation 39
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922557168"
variation 40
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1922557045"
variation 43
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:899949058"
variation 44
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1346564193"
variation 46
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1922556648"
variation 47
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789280"
variation 48
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517789279"
variation 49
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517789277"
variation 52
/gene="MFNG"
/replace=""
/replace="c"
/db_xref="dbSNP:911946038"
variation 52
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:765277336"
variation 55
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789270"
variation 56
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517789267"
variation 57
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789264"
variation 58
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789263"
variation 59
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789260"
variation 63
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789256"
variation 64
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517789255"
variation 65
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922556330"
variation 68
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789253"
variation 69
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789251"
variation 71
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1922556201"
variation 72
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1288052837"
variation 73
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922555911"
variation 75
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517789244"
variation 76
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1348707608"
variation 77
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517789236"
variation 79
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:943876865"
variation 80
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1338228414"
variation 82
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:569270089"
variation 83
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789223"
variation 84
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1922555253"
variation 86
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238053004"
variation 88
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789221"
variation 90
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789215"
variation 91
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517789214"
variation 92
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789210"
variation 93
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:2517789204"
variation 96
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1335160427"
variation 98
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517789197"
variation 99
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922554843"
variation 100
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789193"
variation 102
/gene="MFNG"
/replace=""
/replace="t"
/db_xref="dbSNP:2517789190"
variation 103
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789186"
variation 104
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1322855150"
variation 105
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789183"
variation 106..120
/gene="MFNG"
/replace="tgcc"
/replace="tgccagacttttgcc"
/db_xref="dbSNP:1317726135"
variation 107
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1601803246"
variation 108
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1217579299"
variation 109
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1286482226"
variation 111
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1922554196"
variation 113
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1922554063"
variation 117
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1922553942"
variation 118
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517789171"
variation 119
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517789168"
variation 120
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517789157"
variation 121
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789155"
variation 122
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789153"
variation 123
/gene="MFNG"
/replace=""
/replace="t"
/db_xref="dbSNP:1922553526"
variation 125
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1601803225"
variation 126
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517789147"
variation 127..138
/gene="MFNG"
/replace="ggagcccctgcc"
/replace="ggagcccctgccggagcccctgcc"
/db_xref="dbSNP:1240715442"
variation 127
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789145"
variation 128
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1215408499"
variation 129
/gene="MFNG"
/replace=""
/replace="a"
/db_xref="dbSNP:2517789137"
variation 130
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1046981330"
variation 131
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1307596431"
variation 132
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789132"
variation 134
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1922552416"
variation 137
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517789125"
variation 138..162
/gene="MFNG"
/replace="ctgaccagcttcccctccctgtctg"
/replace="ctgaccagcttcccctccctgtctgaccagcttcccctccctgtctg"
/db_xref="dbSNP:2517789071"
variation 140
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517789119"
variation 142
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789118"
variation 143
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789115"
variation 145
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1490944710"
variation 148
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:41280027"
variation 149
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1029673354"
variation 151
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922552033"
variation 152
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789095"
variation 153
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:1268835310"
variation 155
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:929622316"
variation 156
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517789085"
variation 158
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789084"
variation 160
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751323594"
variation 161
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789076"
variation 162
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:764053492"
variation 164
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789068"
variation 167
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:762821328"
variation 168
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775619432"
variation 169
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1601803193"
variation 171
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:199935726"
variation 172
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274831130"
variation 173..177
/gene="MFNG"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:1335678264"
variation 173
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:759837064"
variation 176
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1922550977"
variation 177
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517789044"
variation 178
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517789042"
variation 182
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1277874232"
variation 183
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145743005"
variation 185
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517789032"
variation 186
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789029"
variation 187
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:777054611"
variation 188
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:377341126"
variation 189
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517789017"
variation 191
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1319514820"
variation 192
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517789012"
variation 194..196
/gene="MFNG"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:769642322"
variation 194
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517789009"
variation 195
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1386730877"
variation 196
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:201649691"
variation 197
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:773476207"
variation 199
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517788997"
variation 201..208
/gene="MFNG"
/replace="ccaa"
/replace="ccaaccaa"
/db_xref="dbSNP:1922548773"
variation 201
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772577955"
variation 202..205
/gene="MFNG"
/replace="caac"
/replace="caacaac"
/db_xref="dbSNP:745727101"
variation 202
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517788988"
variation 204
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:779581899"
variation 205
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:533020931"
variation 206
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1569159687"
variation 207
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:146898721"
misc_feature 208..600
/gene="MFNG"
/inference="COORDINATES:
alignment:Blast2seq::RefSeq|NM_001166343.2"
/note="primary ORF has stop codon >50 nucleotides from the
terminal splice site; nonsense-mediated decay (NMD)
candidate"
variation 208
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:780765208"
variation 209
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:751320824"
variation 211
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1361985381"
variation 215
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:763845941"
variation 216
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1449770141"
variation 217
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:758327571"
variation 218..219
/gene="MFNG"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2517788947"
variation 218
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:752646791"
variation 219
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:201175429"
variation 220
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:368956545"
variation 222
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517788944"
variation 223
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517788939"
variation 224
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922547022"
variation 225
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760996647"
variation 226
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:149231158"
variation 227
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1270826075"
variation 230
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1922546380"
variation 231..232
/gene="MFNG"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2517788921"
variation 231
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922546223"
variation 234
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1232678226"
variation 239
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:748682888"
variation 241
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517788911"
variation 242..257
/gene="MFNG"
/replace="ccctcctcaccctcct"
/replace="ccctcctcaccctcctcaccctcct"
/db_xref="dbSNP:2517788869"
variation 242
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1378134004"
variation 244
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:774777142"
variation 246
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:199731917"
variation 247
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1403531503"
variation 249
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517788894"
variation 250
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517788890"
variation 252
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:77701703"
variation 253..275
/gene="MFNG"
/replace="ctcctgtgcatggggctcctgtg"
/replace="ctcctgtgcatggggctcctgtgcatggggctcctgtg"
/db_xref="dbSNP:2517788817"
variation 253
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922544730"
variation 254
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:1326398026"
variation 255
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:756881144"
variation 256
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1419846332"
variation 258
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517788863"
variation 261
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517788860"
variation 262
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517788854"
variation 263
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:371011196"
variation 264
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:777622307"
variation 266
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517788846"
variation 268
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1396753870"
variation 269
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:758187921"
variation 270
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:752553280"
variation 271..272
/gene="MFNG"
/replace=""
/replace="ct"
/db_xref="dbSNP:781222871"
variation 271
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:778930375"
variation 274
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:149669085"
variation 276..278
/gene="MFNG"
/replace="t"
/replace="tct"
/db_xref="dbSNP:2517788809"
variation 276
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:3177508"
variation 280
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1174070746"
variation 281
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:866227430"
variation 282
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517788803"
variation 284..295
/gene="MFNG"
/replace="acc"
/replace="accacttgaacc"
/db_xref="dbSNP:2517788763"
variation 284
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1274064388"
variation 285
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:866813332"
variation 287
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:753916549"
variation 288
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517788785"
variation 289
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:1437862414"
variation 290
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1015152710"
variation 291
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1235707780"
variation 294
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:766611099"
variation 295
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:8192545"
variation 297
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:750675092"
variation 298
/gene="MFNG"
/replace=""
/replace="t"
/db_xref="dbSNP:1333157928"
variation 298
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:767908801"
variation 299..302
/gene="MFNG"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1922539984"
variation 299
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1922540374"
variation 300
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:762024440"
variation 301
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1376783835"
variation 302
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:200695426"
variation 303
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769102277"
variation 304
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:763501433"
variation 307
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:770496729"
variation 308
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:370413760"
variation 309
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517788715"
variation 310
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517788711"
variation 313
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517788708"
variation 314
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1329380227"
variation 315
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1233610187"
variation 316
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1922538525"
variation 317
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145742710"
variation 318
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517788694"
variation 319
/gene="MFNG"
/replace=""
/replace="a"
/db_xref="dbSNP:2517788691"
variation 319
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:777236155"
variation 320..324
/gene="MFNG"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1211745502"
variation 320
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1408473888"
variation 321
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:771764696"
variation 322
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1046905752"
variation 324
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1282589333"
variation 325
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1336333565"
variation 326
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:747861325"
variation 327
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1278641022"
variation 328
/gene="MFNG"
/replace=""
/replace="c"
/db_xref="dbSNP:2517788666"
variation 328
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1339020474"
variation 329
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517788657"
variation 330
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145742662"
variation 331
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2145742656"
variation 332
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:754940582"
variation 336
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:753863575"
variation 337
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:865941594"
variation 338
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:150961532"
variation 339
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:756204298"
variation 342..345
/gene="MFNG"
/replace="cccg"
/replace="cccgcccg"
/db_xref="dbSNP:758424763"
variation 342
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517788643"
variation 344
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:750527937"
variation 345..348
/gene="MFNG"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:748276804"
variation 345
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201695392"
variation 347
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1922535709"
variation 348
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517788630"
variation 349..353
/gene="MFNG"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:779079999"
variation 350
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1021238506"
variation 351
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:544591245"
variation 352
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1922534821"
variation 353
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517788617"
variation 355
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145742608"
variation 356..368
/gene="MFNG"
/replace="agctaca"
/replace="agctacagctaca"
/db_xref="dbSNP:1922533091"
variation 356
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:866327895"
variation 357
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:751899394"
variation 359
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:577208163"
variation 360
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1922533906"
variation 361
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1164418569"
variation 362
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:147720608"
variation 366
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:144062050"
variation 367
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:770350378"
variation 368
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517788591"
variation 369
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1485615578"
variation 370
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1922532717"
variation 371
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517788581"
variation 372
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:926998646"
variation 373
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517788572"
variation 375
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517788569"
variation 376
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1240800528"
variation 378
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517788562"
variation 378
/gene="MFNG"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2517788566"
variation 379
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517788558"
variation 381
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1218600849"
variation 382
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:774891100"
variation 383
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1477451775"
variation 384
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517788544"
variation 388
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517788541"
variation 390
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145742556"
variation 391
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145742549"
variation 392
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:374078492"
variation 393
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1470355371"
variation 394
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:747879329"
variation 395
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:778815792"
variation 396
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1922531030"
variation 397
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:768635690"
variation 398
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1398787550"
variation 399
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517788519"
variation 400
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517788517"
variation 404
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:949507617"
variation 408
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922530407"
variation 409
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:749222556"
variation 410
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:139281430"
variation 411
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1479314768"
variation 412
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1431421025"
variation 413
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517788497"
variation 415
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1349273356"
variation 416
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:756081585"
variation 417
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517788493"
variation 418
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517788491"
variation 423
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1462878240"
variation 424
/gene="MFNG"
/replace=""
/replace="c"
/db_xref="dbSNP:2517788484"
variation 426
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517788480"
variation 427
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:370324588"
variation 428
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:2517788476"
variation 430
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:566642796"
variation 435
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1427955993"
variation 437
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:781381548"
variation 438
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:757390521"
variation 440..442
/gene="MFNG"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1922528193"
variation 441
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1052305542"
variation 442
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517788460"
variation 443
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1601802751"
variation 449
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:751847953"
variation 454
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1569159521"
variation 455
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:200722579"
variation 456
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:377470737"
variation 457
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1206594077"
variation 458
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517788434"
variation 459
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:770415355"
variation 460
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517788431"
variation 461
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:200265617"
variation 462
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:201944390"
exon 463..565
/gene="MFNG"
/inference="alignment:Splign:2.1.0"
variation 463
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:759305923"
variation 464
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:776319335"
variation 466
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517782711"
variation 467
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:770803089"
variation 469
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1922235189"
variation 470
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760651524"
variation 472..473
/gene="MFNG"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2517782689"
variation 472
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517782694"
variation 475
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517782685"
variation 477
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517782680"
variation 479
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517782678"
variation 480
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1328699088"
variation 481
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517782669"
variation 482
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:773241428"
variation 483
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:772211342"
variation 484
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:529673952"
variation 485
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:748308130"
variation 488
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1327445454"
variation 490..491
/gene="MFNG"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2517782634"
variation 490
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517782638"
variation 491
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:779141270"
variation 492
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:372080629"
variation 493
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:146256245"
variation 494
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:780589744"
variation 495
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517782616"
variation 498
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:756667547"
variation 500
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:540401168"
variation 506
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517782608"
variation 508
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:777408634"
variation 509
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:1254677804"
variation 510
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145735277"
variation 511
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:200767510"
variation 512
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517782589"
variation 513
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:61752256"
variation 517..518
/gene="MFNG"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2517782583"
variation 517
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1298901724"
variation 518
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:764901105"
variation 520
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517782573"
variation 521
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753641999"
variation 523
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1194095196"
variation 525
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1922231562"
variation 527
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517782561"
variation 532
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517782557"
variation 535
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:766197957"
variation 539
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:760606489"
variation 540
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:772013269"
variation 542
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:143472050"
variation 544
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517782540"
variation 545..550
/gene="MFNG"
/replace="ctt"
/replace="cttctt"
/db_xref="dbSNP:780227976"
variation 547
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517782538"
variation 552
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:747671258"
variation 553
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517782530"
variation 556
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:950759145"
variation 558
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:774328330"
variation 559
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1428571616"
variation 561
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517782515"
variation 562
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517782509"
variation 565
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1334790144"
exon 566..719
/gene="MFNG"
/inference="alignment:Splign:2.1.0"
variation 566
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1211475940"
variation 567
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517781513"
variation 570..571
/gene="MFNG"
/replace="t"
/replace="tt"
/db_xref="dbSNP:768115186"
variation 570
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1446731197"
variation 572
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1044276282"
variation 577..586
/gene="MFNG"
/replace=""
/replace="atgtggacga"
/db_xref="dbSNP:2517781483"
variation 577
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:774555565"
variation 580
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:948603633"
variation 584
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:148692414"
variation 585
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:778477744"
variation 589
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1367662317"
variation 591
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517781480"
variation 592
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1292313042"
variation 593
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517781469"
variation 594..596
/gene="MFNG"
/replace="t"
/replace="tat"
/db_xref="dbSNP:2517781458"
variation 594
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1230857663"
variation 595
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:754508062"
variation 597
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:748814125"
variation 602
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:368364230"
variation 603
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:755797620"
variation 604
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:372656414"
variation 608
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517781441"
variation 609
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1922190279"
variation 610
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:144197594"
variation 611
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771342884"
variation 613
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517781427"
variation 617
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1164485670"
variation 620
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517781418"
variation 621
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517781412"
variation 623
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517781401"
variation 624
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517781392"
variation 626
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1601797948"
variation 631
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:749629668"
variation 632
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:781216738"
variation 633..634
/gene="MFNG"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1922189299"
variation 634
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1474243797"
variation 637
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:199788262"
variation 638
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:149568963"
variation 642
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517781360"
variation 643
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517781355"
variation 644
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922188619"
variation 645
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:762874288"
variation 646
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775741057"
variation 647
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:765505658"
variation 648
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465636512"
variation 650
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:540558320"
variation 651
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:138192093"
variation 653
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922187495"
variation 655
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:200778754"
variation 656
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:147087271"
variation 657
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517781314"
variation 658
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:772641442"
variation 661
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:372219546"
variation 664
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2145734153"
variation 665
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1271868915"
variation 666
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:779564449"
variation 667
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1393495920"
variation 668
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1325414856"
variation 670
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517781287"
variation 671
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:201509472"
variation 672
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1922185791"
variation 673
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:745562617"
variation 674
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1922185500"
variation 677
/gene="MFNG"
/replace="c"
/replace="cgc"
/db_xref="dbSNP:1569157594"
variation 678
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:143142978"
variation 679
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1165562615"
variation 680..681
/gene="MFNG"
/replace=""
/replace="gc"
/db_xref="dbSNP:1409512118"
variation 680
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1922184860"
variation 682
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517781251"
variation 683
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:756612988"
variation 685
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1191093163"
variation 686
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:777531879"
variation 688
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:758431344"
variation 690
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1163109140"
variation 692
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:752799622"
variation 698
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1489256471"
variation 699
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517781224"
variation 700
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1265726316"
variation 701
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:765445375"
variation 702
/gene="MFNG"
/replace=""
/replace="c"
/db_xref="dbSNP:2517781216"
variation 702
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1305260543"
variation 703
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1601797829"
variation 704
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1276639554"
variation 705..708
/gene="MFNG"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:2517781207"
variation 706
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759823525"
variation 708
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:575246309"
variation 709
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1601797813"
variation 712
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1922182129"
variation 713
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1922181983"
variation 714
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:373720662"
variation 715
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:760886971"
variation 718
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:773658860"
variation 719
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1317799852"
exon 720..805
/gene="MFNG"
/inference="alignment:Splign:2.1.0"
variation 721
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1266622061"
variation 723
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:762305643"
variation 725
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517778880"
variation 727..735
/gene="MFNG"
/replace=""
/replace="tacagttct"
/db_xref="dbSNP:1555930194"
variation 727
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:199841265"
variation 728
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:764599092"
variation 730
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758928215"
variation 731
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1227463267"
variation 734
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1421269131"
variation 736
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:376317023"
variation 737
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1922070405"
variation 739
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517778851"
variation 743
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1202131929"
variation 744
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1922070067"
variation 745
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1298626545"
variation 746
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:770466294"
variation 747
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1259902611"
variation 748
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1361058207"
variation 750
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1236701574"
variation 751
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:746712436"
variation 753
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1290460374"
variation 753
/gene="MFNG"
/replace="g"
/replace="gg"
/db_xref="dbSNP:769438268"
variation 754
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:772875456"
variation 757
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1303319068"
variation 758
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145731168"
variation 759..760
/gene="MFNG"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2517778818"
variation 765
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:200431061"
variation 769
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:139241915"
variation 770
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517778808"
variation 771
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:554733145"
variation 772
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:199609888"
variation 773
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1569156930"
variation 775
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1217659206"
variation 777
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1922068123"
variation 779
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:749280932"
variation 780
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1922067778"
variation 781
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517778783"
variation 785
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517778781"
variation 787
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1285696110"
variation 789
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1329952048"
variation 791
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1485105575"
variation 795
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:267606242"
variation 796
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:780233047"
variation 797
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:201325626"
variation 798
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517778758"
variation 799
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1390309262"
variation 802
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1192520615"
variation 803
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1159447811"
variation 804
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:750725656"
variation 805
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1922066009"
exon 806..971
/gene="MFNG"
/inference="alignment:Splign:2.1.0"
variation 807
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:540210471"
variation 808
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517776612"
variation 809
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517776610"
variation 811..813
/gene="MFNG"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2517776603"
variation 811
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517776608"
variation 812..816
/gene="MFNG"
/replace=""
/replace="ccgtt"
/db_xref="dbSNP:2517776594"
variation 812
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:781326615"
variation 813
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:757491783"
variation 814
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:187717004"
variation 818
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1921961034"
variation 819
/gene="MFNG"
/replace=""
/replace="a"
/db_xref="dbSNP:2517776589"
variation 819
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517776586"
variation 822
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921960860"
variation 823
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:778149654"
variation 824
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517776577"
variation 825..826
/gene="MFNG"
/replace=""
/replace="g"
/db_xref="dbSNP:1298791334"
variation 825
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145728739"
variation 826
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517776569"
variation 827
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1440711325"
variation 831
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392378246"
variation 832
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758825865"
variation 833
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517776553"
variation 834
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1921959916"
variation 835
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:2145728715"
variation 836
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1325123716"
variation 837
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:905461342"
variation 838
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517776535"
variation 840
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:146856427"
variation 841
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:765671279"
variation 842
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2145728690"
variation 849
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1431512152"
variation 850
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:760161499"
variation 852
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517776518"
variation 856
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1235711425"
variation 859..860
/gene="MFNG"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1294520656"
variation 859
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1921958534"
variation 860
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:745400988"
variation 861
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:574644668"
variation 862
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921958034"
variation 863
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517776494"
variation 867
/gene="MFNG"
/replace="t"
/replace="tt"
/db_xref="dbSNP:2517776492"
variation 868
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921957877"
variation 869
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517776483"
variation 870
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1245131986"
variation 871
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517776473"
variation 873
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:761609677"
variation 874
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:375750639"
variation 875
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517776461"
variation 876
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:774260435"
variation 877
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517776456"
variation 878
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:768564782"
variation 879
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1344918031"
variation 880
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:762788159"
variation 881
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:769624596"
variation 889
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:371348183"
variation 890
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:116786806"
variation 891..916
/gene="MFNG"
/replace="ggccgcctgcagcccagccccctctt"
/replace="ggccgcctgcagcccagccccctcttggccgcctgcagcccagccccc
tctt"
/db_xref="dbSNP:759399628"
variation 891..892
/gene="MFNG"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1352684090"
variation 891
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:367778810"
variation 892
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145728620"
variation 893
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517776414"
variation 894
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:771110031"
variation 895
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1334841289"
variation 896
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517776403"
variation 897
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517776400"
variation 899
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1601794862"
variation 900..910
/gene="MFNG"
/replace="cagccc"
/replace="cagcccagccc"
/db_xref="dbSNP:1569156301"
variation 902
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2145728600"
variation 903
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921955075"
variation 905
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1305631734"
variation 906
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:570555212"
variation 907
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1411182790"
variation 908
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:74729565"
variation 909
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921954131"
variation 910
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758727304"
variation 911
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1047466849"
variation 912
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:753006437"
variation 914
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921953504"
variation 915
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:1921953355"
variation 917
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921953039"
variation 918
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1462705683"
variation 920
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1172987459"
variation 922..924
/gene="MFNG"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:776410615"
variation 924
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:779432544"
variation 925
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517776338"
variation 926
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:755465535"
variation 927
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1484081729"
variation 930
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1253120580"
variation 933
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:2517776327"
variation 934..936
/gene="MFNG"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:770895305"
variation 934
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517776323"
variation 935
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1210828995"
variation 936
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517776310"
variation 939
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517776306"
variation 940
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517776304"
variation 942
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1296733921"
variation 944
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:749933446"
variation 945
/gene="MFNG"
/replace="c"
/replace="caggtccc"
/db_xref="dbSNP:2517776298"
variation 945
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1220239916"
variation 947
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:778219875"
variation 947
/gene="MFNG"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2496621691"
variation 948
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1569156258"
variation 949
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921950565"
variation 950..951
/gene="MFNG"
/replace=""
/replace="ga"
/db_xref="dbSNP:2517776286"
variation 951
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:761556639"
variation 954
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921950234"
variation 955
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:751315740"
variation 956
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517776276"
variation 960
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:763667469"
variation 967
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921949699"
variation 969
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921949562"
exon 972..1057
/gene="MFNG"
/inference="alignment:Splign:2.1.0"
variation 972
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1450618740"
variation 973
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517774007"
variation 977
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921856973"
variation 978
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517773997"
variation 980
/gene="MFNG"
/replace=""
/replace="c"
/db_xref="dbSNP:1170438538"
variation 981
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517773994"
variation 982
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1465058673"
variation 983
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1353379576"
variation 984
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:759455896"
variation 985
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517773979"
variation 986
/gene="MFNG"
/replace=""
/replace="c"
/db_xref="dbSNP:2517773975"
variation 986
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:143008836"
variation 987
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:368218615"
variation 988
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517773964"
variation 990
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517773958"
variation 991
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921856198"
variation 992
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1406303155"
variation 994
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:766304385"
variation 995
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:2517773951"
variation 998..1001
/gene="MFNG"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:2517773939"
variation 998
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921855886"
variation 1000
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:868107470"
variation 1002
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:760702884"
variation 1005
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921855383"
variation 1006
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517773929"
variation 1007
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1312573014"
variation 1008
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:773185213"
variation 1010
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:772318826"
variation 1011
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:748361128"
variation 1012
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:370647226"
variation 1017
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1000180139"
variation 1018
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:769203942"
variation 1019
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517773888"
variation 1021
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921854108"
variation 1022
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517773876"
variation 1023
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:749684241"
variation 1024
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:780641012"
variation 1025
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:543874871"
variation 1027
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1569155695"
variation 1028
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517773848"
variation 1029
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:200159869"
variation 1030
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517773833"
variation 1031
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:746479764"
variation 1034..1055
/gene="MFNG"
/replace="ctccccggaggaggacccctcc"
/replace="ctccccggaggaggacccctcctccccggaggaggacccctcc"
/db_xref="dbSNP:749406574"
variation 1034
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517773824"
variation 1035
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:777187096"
variation 1036..1039
/gene="MFNG"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:2517773797"
variation 1036
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:758063804"
variation 1037
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:752350381"
variation 1039
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:149029040"
variation 1040
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:146430995"
variation 1043
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517773783"
variation 1044
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517773779"
variation 1047
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921852101"
variation 1049..1052
/gene="MFNG"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1435453951"
variation 1050
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1417928918"
variation 1051
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1921851946"
variation 1053
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:1245277474"
variation 1054..1055
/gene="MFNG"
/replace="c"
/replace="cc"
/db_xref="dbSNP:2517773731"
variation 1054
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1177520232"
variation 1056
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517773727"
exon 1058..2024
/gene="MFNG"
/inference="alignment:Splign:2.1.0"
variation 1058
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921737571"
variation 1062
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:8192548"
variation 1063
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:140309148"
variation 1064
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517771284"
variation 1065
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517771283"
variation 1066
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1359306177"
variation 1067
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1440637210"
variation 1070
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1218867082"
variation 1071
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1046538002"
variation 1072
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:890182866"
variation 1073
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1471295883"
variation 1074
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:146713035"
variation 1075
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517771258"
variation 1077
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1182318499"
variation 1081
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517771254"
variation 1082
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1423169173"
variation 1084
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1921735337"
variation 1085
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:776935699"
variation 1086
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145723730"
variation 1087
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517771238"
variation 1089
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1180451627"
variation 1090
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:200753314"
variation 1092
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1483472602"
variation 1093
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1263937774"
variation 1095
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1208325068"
variation 1097
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517771210"
variation 1098
/gene="MFNG"
/replace="t"
/replace="tt"
/db_xref="dbSNP:757895498"
variation 1099
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517771203"
variation 1100
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:143375577"
variation 1103
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517771196"
variation 1104
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517771194"
variation 1105
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517771192"
variation 1106
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1270089752"
variation 1107
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517771184"
variation 1109
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1921733571"
variation 1110
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1239933854"
variation 1111
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517771168"
variation 1114
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1340330159"
variation 1117
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921733133"
variation 1119
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:139606481"
variation 1120
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:749008766"
variation 1123
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1384013732"
variation 1126
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:779815995"
variation 1128
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1455288339"
variation 1130
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517771141"
variation 1132
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:755810977"
variation 1135
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:750238306"
variation 1136
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1398985555"
variation 1137..1153
/gene="MFNG"
/replace="tgggcaaaggttgggca"
/replace="tgggcaaaggttgggcaaaggttgggca"
/db_xref="dbSNP:763628395"
variation 1137
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1569154928"
variation 1138
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1456974163"
variation 1139
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:780952028"
variation 1141
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:757243577"
variation 1143
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424378511"
variation 1145
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1247154479"
variation 1146
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1053313861"
variation 1149
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517771109"
variation 1150
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:559707662"
variation 1151
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1463704061"
variation 1153
/gene="MFNG"
/replace=""
/replace="a"
/db_xref="dbSNP:752124888"
variation 1153
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:764334080"
variation 1156
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1205719757"
variation 1161
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1355764485"
variation 1163
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517771093"
variation 1164
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1233126093"
variation 1167
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:941910187"
variation 1168
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1247598324"
variation 1170
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1360842927"
variation 1174
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:936224007"
variation 1175
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:763253603"
variation 1176
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517771075"
variation 1178
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1569154900"
variation 1179
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1433420235"
variation 1180
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1366834732"
variation 1181
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145723599"
variation 1182
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:752908199"
variation 1184
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517771062"
variation 1187
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:567242539"
variation 1188
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1387926508"
variation 1190
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:759775653"
variation 1193
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921728672"
variation 1194..1199
/gene="MFNG"
/replace=""
/replace="gggtcc"
/db_xref="dbSNP:1245414121"
variation 1198
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921728544"
variation 1199
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1198579551"
variation 1200
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517771036"
variation 1201..1202
/gene="MFNG"
/replace=""
/replace="tgtgata"
/db_xref="dbSNP:1442058014"
variation 1203
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517771032"
variation 1204
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:777073480"
variation 1205
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921727874"
variation 1207..1210
/gene="MFNG"
/replace="gt"
/replace="gtgt"
/db_xref="dbSNP:1921727515"
variation 1207
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1389547445"
variation 1208
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:1921727646"
variation 1211
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1166424179"
variation 1214
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921727276"
variation 1218
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921727146"
variation 1219..1228
/gene="MFNG"
/replace=""
/replace="aggcagtccc"
/db_xref="dbSNP:2517770988"
variation 1221
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1451099855"
variation 1222
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517770998"
variation 1224
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:771316864"
variation 1226
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921726714"
variation 1227..1230
/gene="MFNG"
/replace="cctg"
/replace="cctgcctg"
/db_xref="dbSNP:1223211570"
variation 1228
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921726591"
variation 1230
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921726312"
variation 1231
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1281045587"
variation 1232
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1601791589"
variation 1234
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1194192735"
variation 1235
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517770964"
variation 1236
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921725817"
variation 1241
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:761281874"
variation 1242
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1322610949"
variation 1243
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:928021763"
variation 1244
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1265318706"
variation 1246
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145723482"
variation 1247
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1280099349"
variation 1248
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1211778654"
variation 1250
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770946"
variation 1255
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1490652379"
variation 1256..1258
/gene="MFNG"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2517770932"
variation 1256
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1274568946"
variation 1257
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921724928"
variation 1260
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770929"
variation 1261
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770924"
variation 1263
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:2517770921"
variation 1267
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:773849305"
variation 1270
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770916"
variation 1271
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1370416329"
variation 1272
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:760335560"
variation 1274
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770908"
variation 1276
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:748814181"
variation 1277
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517770905"
variation 1278
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770899"
variation 1279
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:573795847"
variation 1281
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1921724158"
variation 1282
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921724022"
variation 1283
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770889"
variation 1286
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517770887"
variation 1287
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:769517608"
variation 1290
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517770883"
variation 1293
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:987918829"
variation 1294
/gene="MFNG"
/replace=""
/replace="a"
/db_xref="dbSNP:1921723387"
variation 1296
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1405048492"
variation 1297..1300
/gene="MFNG"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1601791527"
variation 1297
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1369806209"
variation 1298
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:950866133"
variation 1299
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1357317189"
variation 1300
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306135776"
variation 1302..1307
/gene="MFNG"
/replace="gg"
/replace="gggagg"
/db_xref="dbSNP:2517770851"
variation 1302..1304
/gene="MFNG"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:2517770864"
variation 1304
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:745602143"
variation 1305
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770857"
variation 1306
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517770853"
variation 1309
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1396912212"
variation 1311
/gene="MFNG"
/replace=""
/replace="g"
/db_xref="dbSNP:1171823231"
variation 1311
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517770843"
variation 1313
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921721674"
variation 1314..1319
/gene="MFNG"
/replace="ag"
/replace="agacag"
/db_xref="dbSNP:1209514280"
variation 1314
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921721473"
variation 1317
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517770836"
variation 1320..1322
/gene="MFNG"
/replace="cc"
/replace="ccc"
/db_xref="dbSNP:2517770828"
variation 1320
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:775448603"
variation 1321
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517770829"
variation 1322
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517770824"
variation 1325
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1569154841"
variation 1326..1345
/gene="MFNG"
/replace="ggaccaggtgg"
/replace="ggaccaggtggaccaggtgg"
/db_xref="dbSNP:1921719852"
variation 1326
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517770818"
variation 1327
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:561885129"
variation 1330
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1179694672"
variation 1332..1333
/gene="MFNG"
/replace="g"
/replace="gg"
/db_xref="dbSNP:2517770807"
variation 1334
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238036959"
variation 1335
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770803"
variation 1336
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517770799"
variation 1339
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:765606428"
variation 1340
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770795"
variation 1341
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517770792"
variation 1343..1345
/gene="MFNG"
/replace="tgg"
/replace="tggaccagctgg"
/db_xref="dbSNP:1179033476"
variation 1344
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770788"
variation 1347
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1251758903"
variation 1348
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:973234917"
variation 1351
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1601791470"
variation 1357
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517770765"
variation 1360
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517770761"
variation 1362
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517770760"
variation 1365
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517770758"
variation 1366
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1569154822"
variation 1368
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1229499735"
variation 1369
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:958506368"
variation 1373
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:963202499"
variation 1374
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921718675"
variation 1376
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1391872252"
variation 1381
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770745"
variation 1383
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145723363"
variation 1386
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:543393412"
variation 1388..1389
/gene="MFNG"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1921718256"
variation 1390
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1300306780"
variation 1393
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1441208763"
variation 1398
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517770732"
variation 1400
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1002136258"
variation 1401
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517770729"
variation 1403..1407
/gene="MFNG"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:2517770720"
variation 1403
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:970760282"
variation 1405
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517770725"
variation 1406
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517770722"
variation 1407
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1314903803"
variation 1414
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145723331"
variation 1416
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1341197265"
variation 1420
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1244186190"
variation 1424
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770712"
variation 1426
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:866271473"
variation 1429
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1009723203"
variation 1430
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770706"
variation 1434
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:995845230"
variation 1435
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:900174470"
variation 1437
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2517770698"
variation 1440
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921715964"
variation 1444
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:892249412"
variation 1445
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517770689"
variation 1449
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517770682"
variation 1450
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921715712"
variation 1457
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:1921715597"
variation 1459
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1328697035"
variation 1462
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921715465"
variation 1466
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1202753884"
variation 1467
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770663"
variation 1468
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1257504853"
variation 1471
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1921715083"
variation 1472
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921714949"
variation 1473
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1601791394"
variation 1476
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921714695"
variation 1479..1480
/gene="MFNG"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1921714422"
variation 1479
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921714556"
variation 1480
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:116600298"
variation 1481
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1396579009"
variation 1482
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921713967"
variation 1484
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921713790"
variation 1485
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517770622"
variation 1487
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921713638"
variation 1488
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517770620"
variation 1491
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1415135837"
variation 1493
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1000340869"
variation 1495
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:759589441"
variation 1497
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478631018"
variation 1498..1503
/gene="MFNG"
/replace="tctc"
/replace="tctctc"
/db_xref="dbSNP:2517770602"
variation 1501
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517770604"
variation 1503
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:941978085"
variation 1507
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:904703193"
variation 1508
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770594"
variation 1511
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1039267136"
variation 1513
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921712614"
variation 1514
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921712484"
variation 1516..1519
/gene="MFNG"
/replace="gggg"
/replace="ggggg"
/db_xref="dbSNP:2517770578"
variation 1517
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517770580"
variation 1518
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921712354"
variation 1519
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:907766415"
variation 1520
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1304467039"
variation 1521
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1169068941"
variation 1526
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:187947852"
variation 1527
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1047587144"
variation 1528
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:943634534"
variation 1529
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517770560"
variation 1534
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:539366080"
variation 1535
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:911876876"
variation 1539
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1255047134"
variation 1540
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517770543"
variation 1543
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921710767"
variation 1544
/gene="MFNG"
/replace=""
/replace="t"
/db_xref="dbSNP:2145723198"
variation 1547
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517770537"
variation 1549
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:982199273"
variation 1552
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517770529"
variation 1553
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921710496"
variation 1562
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1601791340"
variation 1564
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:572164168"
variation 1565
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:35852296"
variation 1567
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921710083"
variation 1571
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:535695342"
variation 1572
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921709812"
variation 1576..1578
/gene="MFNG"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1489048437"
variation 1577
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770504"
variation 1579
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1251327572"
variation 1580
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:2145723168"
variation 1581
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1422502421"
variation 1583..1585
/gene="MFNG"
/replace="gg"
/replace="ggg"
/db_xref="dbSNP:1921709244"
variation 1585
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921709118"
variation 1593
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:140730359"
variation 1594
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1177973794"
variation 1595
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1378079299"
variation 1605
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921708653"
variation 1606
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:549930944"
variation 1607
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921708317"
variation 1608
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1362586076"
variation 1613
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:754010433"
variation 1622
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921708036"
variation 1624
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:973472592"
variation 1627
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1921707782"
variation 1630
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921707638"
variation 1634
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1297774268"
variation 1635
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1360135755"
variation 1638
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770447"
variation 1642
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1388829028"
variation 1644
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517770442"
variation 1648
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921707105"
variation 1650
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:2517770437"
variation 1651
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1302481862"
variation 1653
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1312116556"
variation 1659
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2517770432"
variation 1664
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1342727304"
variation 1665
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1921706602"
variation 1667..1668
/gene="MFNG"
/replace="t"
/replace="tt"
/db_xref="dbSNP:1232790562"
variation 1670
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1031660844"
variation 1671
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:537821272"
variation 1673
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:954880535"
variation 1674
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1030424198"
variation 1679
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1349621738"
variation 1681
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2145723073"
variation 1684
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:1921705715"
variation 1689
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1306706216"
variation 1691
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1921705434"
variation 1696
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921705294"
variation 1697
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1921705159"
variation 1699
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1238973883"
variation 1703
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1192697860"
variation 1705
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1601791255"
variation 1706
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1267883493"
variation 1707..1734
/gene="MFNG"
/replace="cggg"
/replace="cggggcccagatgatggagcataacggg"
/db_xref="dbSNP:1921702908"
variation 1707
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:368245526"
variation 1708
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:981094434"
variation 1709
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:970704083"
variation 1711
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1171624079"
variation 1712
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:900227157"
variation 1715
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1921703889"
variation 1718
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1601791238"
variation 1719
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1921703615"
variation 1725
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1420308808"
variation 1727
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:183450873"
variation 1731
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1025047851"
variation 1732
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:552012311"
variation 1736
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:987846870"
variation 1737
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1312657730"
variation 1738
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1459700836"
variation 1741
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:2517770365"
variation 1744
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:2517770362"
variation 1750
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:886393243"
variation 1751
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1047680100"
variation 1755..1756
/gene="MFNG"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1435663179"
variation 1755
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1367402581"
variation 1756
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921701825"
variation 1757
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:938545373"
variation 1759
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:533462897"
variation 1764
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145722967"
variation 1771
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921701490"
variation 1772
/gene="MFNG"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:138795813"
variation 1774
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:956377107"
variation 1775
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1283019259"
variation 1779
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1314765395"
variation 1780
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1223372369"
variation 1785
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1032064503"
variation 1787..1788
/gene="MFNG"
/replace="tt"
/replace="ttt"
/db_xref="dbSNP:1921700518"
variation 1789
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1000623917"
variation 1791
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:547577975"
variation 1794
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921700397"
variation 1796
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921700277"
variation 1797
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1017808594"
variation 1798
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1239866864"
variation 1799
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:748187261"
variation 1800
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921699730"
variation 1805
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1440302642"
variation 1806
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:377059655"
variation 1810
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921699322"
variation 1813
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:948183702"
variation 1815
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:916638005"
variation 1817
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1165688830"
variation 1818
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:537486258"
variation 1822
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:528710760"
variation 1830
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1333808282"
variation 1839
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921698501"
variation 1842
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1052466007"
variation 1844
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921698203"
variation 1847
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:1921698065"
variation 1852..1855
/gene="MFNG"
/replace="ggg"
/replace="gggg"
/db_xref="dbSNP:2145722880"
variation 1852
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1211495154"
variation 1855
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1446784586"
variation 1865
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1278418801"
variation 1871
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:923928147"
variation 1880
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921697380"
variation 1884
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1229565038"
variation 1889
/gene="MFNG"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:543529693"
variation 1891
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:55698891"
variation 1893
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:897838898"
variation 1898
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921696616"
variation 1900
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921696430"
variation 1901
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:954931294"
variation 1903
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1030477831"
variation 1908
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921695745"
variation 1912
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1601791104"
variation 1914
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:564331222"
variation 1925
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1601791100"
variation 1929
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921694977"
variation 1931
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1259825589"
variation 1935
/gene="MFNG"
/replace="c"
/replace="g"
/db_xref="dbSNP:1350876536"
variation 1936
/gene="MFNG"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1921694556"
variation 1938
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:546030759"
variation 1942
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1280812043"
variation 1947
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921694139"
variation 1956
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1241898296"
variation 1959
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:572248215"
variation 1972
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921693606"
variation 1973
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:2145722815"
variation 1985..1986
/gene="MFNG"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1921693477"
variation 1986
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921693343"
variation 1994
/gene="MFNG"
/replace="a"
/replace="c"
/db_xref="dbSNP:1921693211"
variation 1995
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921693096"
variation 1996
/gene="MFNG"
/replace="a"
/replace="g"
/db_xref="dbSNP:1921692961"
variation 2002
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:1921692804"
variation 2005
/gene="MFNG"
/replace="a"
/replace="t"
/db_xref="dbSNP:1037711993"
variation 2008
/gene="MFNG"
/replace="g"
/replace="t"
/db_xref="dbSNP:1473795837"
variation 2009
/gene="MFNG"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:974864937"
variation 2011
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:1921692229"
variation 2015
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:942158681"
variation 2022
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:964521606"
variation 2024
/gene="MFNG"
/replace="c"
/replace="t"
/db_xref="dbSNP:764722326"
ORIGIN
agcaggtggaggactggcggcggtcgagatcgtgctgccatggctcagcctctgggtccagagcctcagctcctacctcttccctccttgccagcccctgatgcctgccagacttttgcctctgctggagcccctgcctgaccagcttcccctccctgtctggttgggatttgggggctgagctgtctggggtcccagggccaaccaatgcagtgccggctcccgcggggcctggctggagccctcctcaccctcctgtgcatggggctcctgtgtctgcggtaccacttgaacctgtccccgcagcgggtacaagggacccccgagctgagccagccgaacccggggccccctaagctacagctacacgatgtcttcattgcagtgaagacgacccgggctttccaccgcttgcgcctggagctgctgcttgacacgtgggtttccaggaccagggaacagggtcccaccttgtggtcaccaactgctccgcggaacacagccacccagctctgtcctgcaagatggctgctgagttcgacaccttcttggccagtgggcttaggtggttctgccatgtggacgatgacaactatgtgaacccaagggcgctgctgcagcttctgagagccttcccgctggcccgcgacgtctatgtgggaaggcccagcctgaaccggcccatccatgcctcagagccacagccccacaaccgcacgaggctggtacagttctggtttgccactgggggtgctggcttctgcatcaatcgcaaactggctttgaagatggctccgtgggccagtggctcccgtttcatggacacatctgctctcatccggctgcctgatgactgcaccatgggctatatcattgagtgcaagctgggcggccgcctgcagcccagccccctctttcactcccacctggagaccctgcagctgctgaggactgcacagctcccagaacaggtcaccctcagctacggtgtctttgaggggaaactcaacgtcattaagctacagggccccttctccccggaggaggacccctccagatttcgctccctccattgtctgctctatccagatacaccctggtgtccccagctgggtgcccgatgaatcctgaactgctgggcaaaggttgggcagagacttctgggtgtgccttggctcccaaggtggcactgtgggtccctggcaagtgtcttgtgataggcagtccctggcagggccttcgggtggttggcaagcccaggatctgagtggcaattggcactgaaggcaccccaggcccctgggaggtgagttagacagcccaggggaccaggtggaccaggtggtggccagagaggctccaggggctagactccctcaggaggctgaattgaaaaagggcagggggcacttgagctgggctggggctcaggggtcctaaccctttaggcagtgacatggcctctgggtggggtctggccgttggccctggctaatgtctctcagtcattcccctggggctcaagcgctgggccgcccactcctgcctccctcatctgtgtcccgagttcctgaagggacatgggtggaatgatggcagaatccagggtctgcagcacctgctgttgttgccaaccagtctcccaaagctccttgctccccaccccttgcgaacaggaccagattttgtttggagcctcagcatgccggggcccagatgatggagcataacgggtcccagccaattgtgatgatcctttttgctcatttcccagcctttcttgctgttaggggctaccatgggaccagctctggccagagggaactaagcaaatccaatagagatgtttctggggaaggttttgcagcccactccccatcttcctgctataaatgtgggtgtgatggctggatctggggcagccaccttgctaccatgaaggaaaggccaagacaatcatccacagctattccctccagcatctggttctgtacaaaaattaaatgcttatttgtttaagtctc
//
by
@meso_cacase at
DBCLS
This page is licensed under a
Creative Commons Attribution 4.0 International License (CC BY 4.0).
If you use GGRNA in your work, please cite:
Naito Y, Bono H. (2012)
GGRNA: an ultrafast, transcript-oriented search engine for genes and transcripts.
Nucleic Acids Res., 40, W592-W596.
[Full Text]