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Previous release (v1)
2024-05-02 06:46:37, GGRNA.v2 : RefSeq release 222 (Jan, 2024)
LOCUS NR_003720 779 bp RNA linear PRI 19-APR-2022
DEFINITION Homo sapiens casein alpha s2 like A, pseudogene (CSN1S2AP),
non-coding RNA.
ACCESSION NR_003720 XM_379270 XM_943523
VERSION NR_003720.1
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 779)
AUTHORS Rijnkels M, Elnitski L, Miller W and Rosen JM.
TITLE Multispecies comparative analysis of a mammalian-specific genomic
domain encoding secretory proteins
JOURNAL Genomics 82 (4), 417-432 (2003)
PUBMED 13679022
REFERENCE 2 (bases 1 to 779)
AUTHORS Rijnkels M.
TITLE Multispecies comparison of the casein gene loci and evolution of
casein gene family
JOURNAL J Mammary Gland Biol Neoplasia 7 (3), 327-345 (2002)
PUBMED 12751895
REMARK Review article
COMMENT VALIDATED REFSEQ: This record has undergone validation or
preliminary review. The reference sequence was derived from
AY154892.1.
On or before Sep 11, 2007 this sequence version replaced
XM_379270.4, XM_943523.2.
Summary: This locus is the equivalent of casein gamma in mouse
(GeneID 12993) and is found in a cluster of casein genes, similar
to other mammals. In human, the potential open reading frame that
matches the homologous protein from other species is prematurely
truncated shortly after the signal peptide. Therefore, this locus
appears to be a pseudogene. [provided by RefSeq, Jul 2008].
##Evidence-Data-START##
Transcript exon combination :: AY154892.1 [ECO:0000332]
RNAseq introns :: single sample supports all introns
SAMN02400288, SAMN02400308
[ECO:0000348]
##Evidence-Data-END##
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-779 AY154892.1 1-779
FEATURES Location/Qualifiers
source 1..779
/organism="Homo sapiens"
/mol_type="transcribed RNA"
/db_xref="taxon:9606"
/chromosome="4"
/map="4q13.3"
gene 1..779
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/note="casein alpha s2 like A, pseudogene"
/pseudo
/db_xref="GeneID:286828"
/db_xref="HGNC:HGNC:20230"
misc_RNA 1..779
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/product="casein alpha s2 like A, pseudogene"
/pseudo
/db_xref="GeneID:286828"
/db_xref="HGNC:HGNC:20230"
exon 1..44
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 4
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:2109738891"
variation 10
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:2109738894"
variation 11
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:375004172"
variation 12
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1361484119"
variation 13
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1487395167"
variation 15
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1286627635"
variation 18
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:552444305"
variation 19
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:927298346"
variation 20
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1726298919"
variation 23
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726298975"
variation 24
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1726299018"
variation 30
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:938640529"
variation 38
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726299118"
variation 41
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1726299170"
exon 45..107
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 45
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1726344347"
variation 50
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1371852213"
variation 51
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:569993426"
variation 52
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1054388443"
variation 53
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1299122800"
variation 55
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1167839337"
variation 56
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1309115308"
variation 59
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:865862883"
variation 61
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1205037599"
variation 64
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1250539737"
variation 65
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1479483648"
variation 69
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1215145249"
variation 70
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:766108319"
variation 71
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:145418379"
variation 73
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1191148542"
variation 75
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:555853023"
variation 77
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:943413402"
variation 81
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1726345391"
variation 86
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726345441"
variation 87
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1040334915"
variation 90
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="gg"
/db_xref="dbSNP:752206775"
variation 95
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1171616930"
variation 98..99
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="gg"
/db_xref="dbSNP:1372832497"
variation 99
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1269359383"
variation 100
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:147671055"
variation 101
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1464350965"
variation 102
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328197372"
variation 106
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1428289236"
variation 107
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1480171880"
exon 108..137
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 108
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1416400400"
variation 117
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1726382155"
variation 118
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1560440993"
variation 119..127
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="ctcctc"
/replace="ctcctcctc"
/db_xref="dbSNP:748876420"
variation 121
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:972927019"
variation 122
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1293677368"
variation 124
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1333780279"
variation 125
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1358036642"
variation 127
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1315071870"
variation 128
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1226225192"
variation 130..131
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="cc"
/db_xref="dbSNP:1285865117"
variation 131
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:917052788"
variation 132
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:17148025"
variation 133
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1726383583"
variation 134..136
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="tga"
/replace="tgatga"
/db_xref="dbSNP:1726383768"
variation 134
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1299696674"
variation 137
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1726383848"
exon 138..161
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 138
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:2109741831"
variation 144
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1726403732"
variation 145
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726403798"
variation 146
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1578190098"
variation 148
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1560441243"
variation 151
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:532490927"
variation 153
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:184294431"
variation 159
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1045041450"
exon 162..188
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 162
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1406818733"
variation 164
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1442229468"
variation 165
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1465202068"
variation 168
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1208387264"
variation 172
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:2109742742"
variation 173
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726438324"
variation 178
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1234822902"
variation 181
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1386475421"
variation 183
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1408717277"
variation 184
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:749470844"
variation 185
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:775773815"
variation 187
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:548065916"
exon 189..215
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 190
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:370990485"
variation 192
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:760332813"
variation 193
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1372525413"
variation 196
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:938831788"
variation 197
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1296426228"
variation 200
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726455843"
variation 203
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1057513237"
variation 206
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726455992"
variation 208
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:913482085"
variation 209
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:2109743071"
variation 210
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1339533473"
variation 211
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1560441838"
variation 212
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726456340"
variation 213
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726456404"
variation 214
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:945061502"
variation 215
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:17148039"
exon 216..239
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 218
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1177366238"
variation 219
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:190085307"
variation 220
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:926008468"
variation 230
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1041826593"
variation 231
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1053210111"
variation 232
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:867702461"
variation 234
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1726487280"
variation 234
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:890598169"
variation 235
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1396150048"
variation 236
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:2109743958"
exon 240..284
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 240
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1461629825"
variation 243
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1726490862"
variation 244
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:760776568"
variation 245
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1162182549"
variation 246
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:766380196"
variation 248..254
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="act"
/replace="actgact"
/db_xref="dbSNP:1383361102"
variation 249
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:751330869"
variation 258
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1160988090"
variation 262
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:2109744032"
variation 265
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1005016639"
variation 266
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1726492201"
variation 267
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1399852320"
variation 272
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1726492309"
variation 273
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1276682833"
variation 275
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1337285784"
variation 277
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1234097113"
variation 278
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:539582859"
variation 281
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:2109744050"
variation 282
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1368284324"
exon 285..308
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 285
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1352963386"
variation 288
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:2109747701"
variation 291
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:921585197"
variation 293
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1578193033"
variation 296
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1214324027"
variation 301
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:758639852"
variation 304
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726630089"
variation 305
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1485882057"
exon 309..332
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 309
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1237138127"
variation 310
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:879109607"
variation 312
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1726663299"
variation 315
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:775200567"
variation 318
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1194886731"
variation 319
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1726663403"
variation 322
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1163013146"
variation 324
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726663600"
variation 327
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1397506718"
variation 328
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1434246998"
variation 330
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1175857825"
variation 332
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:943977064"
exon 333..456
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 333
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1363905257"
variation 334
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400455885"
variation 335
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1011981764"
variation 336
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1181883100"
variation 337
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1435390693"
variation 340
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:985091763"
variation 341
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1338032862"
variation 345
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:1726701941"
variation 349
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1017581697"
variation 352
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726702039"
variation 353
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:964811102"
variation 354
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:997575792"
variation 356
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:2109749736"
variation 361
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1320620384"
variation 364
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace=""
/replace="c"
/db_xref="dbSNP:1726702297"
variation 364
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:2109749740"
variation 368..372
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="cccc"
/replace="ccccc"
/db_xref="dbSNP:1421415890"
variation 368
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1578194082"
variation 370
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1218671198"
variation 373
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:2109749751"
variation 382
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1264213436"
variation 383
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1487126721"
variation 384
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1726703403"
variation 387
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1726703441"
variation 388
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1181672027"
variation 390..393
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="ccc"
/replace="cccc"
/db_xref="dbSNP:1194905533"
variation 390
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726703554"
variation 394
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1262878895"
variation 396..400
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="gt"
/replace="gtagt"
/db_xref="dbSNP:1477022260"
variation 397
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1578194100"
variation 399
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726703979"
variation 400
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1030535559"
variation 403
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:752820615"
variation 404
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:2109749773"
variation 405
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1189699589"
variation 406
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1414728366"
variation 407
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726704231"
variation 408
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:950931745"
variation 415
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:983760803"
variation 421
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:909448598"
variation 428..437
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace=""
/replace="aaaacaccta"
/db_xref="dbSNP:1726704673"
variation 428..434
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace=""
/replace="aaaacac"
/db_xref="dbSNP:1726704614"
variation 428
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1420211093"
variation 432
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726704727"
variation 433
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1560445131"
variation 434
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1297400352"
variation 437..439
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace=""
/replace="acc"
/db_xref="dbSNP:1726704909"
variation 437
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1358426262"
variation 439
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726704966"
variation 440
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1213485676"
variation 441
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:963629191"
variation 442
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:2109749801"
variation 444
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1284442432"
variation 448
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1377911766"
variation 449
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1226172278"
variation 454
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:758792593"
variation 456
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:973712921"
exon 457..502
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 459
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:947283650"
variation 461
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726743623"
variation 462
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1391493220"
variation 463
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726743782"
variation 464
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:2109750780"
variation 465
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:182844962"
variation 466..482
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="taa"
/replace="taagattcttgaattaa"
/db_xref="dbSNP:1726743873"
variation 467
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1392557892"
variation 469
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:940698604"
variation 470
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1189855043"
variation 473
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1578194624"
variation 476
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1454059563"
variation 477
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:375126061"
variation 478
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1478953561"
variation 480
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1172980863"
variation 481
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1424237371"
variation 483
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1412492076"
variation 484
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726744766"
variation 485
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726744838"
variation 486
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:114149975"
variation 489
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400486732"
variation 492
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:920685281"
variation 493
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1328672690"
variation 495
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1726745288"
variation 497
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1290192139"
variation 501
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1051566850"
variation 502
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1439186043"
exon 503..779
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/inference="alignment:Splign:2.1.0"
/pseudo
variation 507
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:570708869"
variation 509
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1316256891"
variation 511
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726816194"
variation 512
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace=""
/replace="g"
/db_xref="dbSNP:940533043"
variation 512
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:148025945"
variation 516
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1377391687"
variation 519
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1336274928"
variation 520
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1726816684"
variation 522
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:2109752346"
variation 523
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:538247914"
variation 525
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1450682113"
variation 530
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1408634210"
variation 534
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:749968344"
variation 542
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726817040"
variation 544
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1033792142"
variation 547
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1578195467"
variation 548
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726817246"
variation 549
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1726817290"
variation 551
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1726817324"
variation 552
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:2109752363"
variation 555
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:959049296"
variation 559
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace=""
/replace="c"
/db_xref="dbSNP:917798469"
variation 559
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1420002306"
variation 560
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:549971089"
variation 568
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726817558"
variation 572
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726817598"
variation 575
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:947976334"
variation 580
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:186004587"
variation 581
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726817766"
variation 582
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726817802"
variation 583
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726817853"
variation 586
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1200530385"
variation 588
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1262432012"
variation 589
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726818009"
variation 591
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1024716824"
variation 599
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace=""
/replace="t"
/db_xref="dbSNP:1726818105"
variation 600
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:2109752389"
variation 603
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1258839328"
variation 605
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1726818194"
variation 606
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726818239"
variation 608..611
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="aaa"
/replace="aaaa"
/db_xref="dbSNP:1241134648"
variation 608
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:966827196"
variation 616
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726818435"
variation 618
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1726818501"
variation 621
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:536037431"
variation 626
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1560446525"
variation 627
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1314081927"
variation 628
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726818696"
variation 630..664
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="tttccatattggttatgatatttttaatttgtgtt"
/replace="tttccatattggttatgatatttttaatttgtgtttccatattggtta
tgatatttttaatttgtgtt"
/db_xref="dbSNP:1206844299"
variation 632
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1578195485"
variation 633
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:545222816"
variation 634
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1385253166"
variation 637
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1335105589"
variation 638
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726819079"
variation 639
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1578195490"
variation 644..648
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="at"
/replace="atgat"
/db_xref="dbSNP:1726819315"
variation 644
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:191163486"
variation 646
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:2109752430"
variation 649
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726819400"
variation 650
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:936029120"
variation 652
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1726819567"
variation 655
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1427741215"
variation 659
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1199664378"
variation 662
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1726819816"
variation 667
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726819871"
variation 671
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1726819927"
variation 673
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:181809512"
variation 683
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/replace="t"
/db_xref="dbSNP:17644794"
variation 684
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1175000260"
variation 685
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1010403706"
variation 687
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726820569"
variation 688
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1363890931"
variation 695
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:2109752464"
variation 699
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:2109752465"
variation 700
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726820743"
variation 701
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1187832992"
variation 708
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:911252525"
variation 716
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:902071238"
variation 718
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/replace="t"
/db_xref="dbSNP:1578195515"
variation 722
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:185389481"
variation 723
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1383221592"
variation 724..727
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="ttt"
/replace="tttt"
/db_xref="dbSNP:2109752486"
variation 726
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="g"
/replace="t"
/db_xref="dbSNP:1726821380"
variation 727
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726821451"
variation 728..731
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="ctcc"
/db_xref="dbSNP:1726821622"
variation 728
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:1041410344"
variation 733
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1291030359"
variation 734
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726821763"
variation 735
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:1219889469"
variation 737
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726821923"
variation 738
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:576724822"
variation 739
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/db_xref="dbSNP:755548393"
variation 741
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726822186"
variation 745
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1284953619"
variation 747
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1399836020"
variation 749
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:544213699"
variation 750..751
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="aa"
/db_xref="dbSNP:1486575511"
variation 750
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1048556691"
variation 752
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:888601569"
variation 754
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1001765297"
variation 755
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1400753676"
variation 756
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1726823065"
variation 760
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="g"
/db_xref="dbSNP:1726823127"
variation 762
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1726823172"
variation 763
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1560446572"
variation 764..772
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace=""
/replace="tgccaaaac"
/db_xref="dbSNP:144478334"
variation 771
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1301842519"
variation 772
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="c"
/replace="t"
/db_xref="dbSNP:1726823408"
variation 773
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1726823472"
variation 774
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="c"
/replace="t"
/db_xref="dbSNP:1426884804"
variation 776
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="t"
/db_xref="dbSNP:1056045589"
variation 778
/gene="CSN1S2AP"
/gene_synonym="CSN1S2A"
/replace="a"
/replace="g"
/db_xref="dbSNP:1347696785"
ORIGIN
attttccactgtgtagtccactggtcttctatttgggaaacaaggaccaaacaaccatgaagttcttcatctttacctgccttttggctgttgctctggcacatcatgagataaagcactcctcctcttccagtgagtaatctgccagcatctaccaagaagaaactgcaaataaaatagatacgatgcaatcttctagcagtttatccagtggggaatctgctcaagtatccactgaaaacaatgaactgactaaggaaggaaggatctacttaaagcacatggaatctaccagcatctcccaagaagaatctgctgaagtattccctgagacgaaaaccaaccagtttctccagaagttcactgtcccccagtatgtccaggctgttccccttgtagtctatgagcctgtggaatcacattcaggaaaacacctacccatatattcccatttagaagaacatgtaagattcttgaattaactgctgcaatttgagcttgagtatgactagaaaaatcattcctttataatttcttcatctaccacatcacctcctactagcaatatattttggcatgcttcttgaaatgtcaacagtattgagccaaaagaagactgtgtggaacattttccatattggttatgatatttttaatttgtgttggatatgccagatctgaattgtggtatcatatttactgtattgatgattaaatgaggtcttttctccactatctctgaaatatagaactgtatatcagttgccaaaacattaaaa
//
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]