2024-12-03 09:02:56, GGRNA.v2 : RefSeq release 226 (Sep, 2024)
LOCUS NM_001017361 1037 bp mRNA linear PRI 17-MAR-2024 DEFINITION Homo sapiens KH domain containing 3 like, subcortical maternal complex member (KHDC3L), mRNA. ACCESSION NM_001017361 XM_087901 VERSION NM_001017361.3 KEYWORDS RefSeq; MANE Select. 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 1037) AUTHORS Rath,A., Sethi,P., Jena,S.K. and Mitra,S. TITLE Familial recurrent molar pregnancy: positive for KHDC3L gene mutation JOURNAL BMJ Case Rep 16 (11), e254435 (2023) PUBMED 37918946 REMARK GeneRIF: Familial recurrent molar pregnancy: positive for KHDC3L gene mutation. Publication Status: Online-Only REFERENCE 2 (bases 1 to 1037) AUTHORS Pignata,L., Cecere,F., Verma,A., Hay Mele,B., Monticelli,M., Acurzio,B., Giaccari,C., Sparago,A., Hernandez Mora,J.R., Monteagudo-Sanchez,A., Esteller,M., Pereda,A., Tenorio-Castano,J., Palumbo,O., Carella,M., Prontera,P., Piscopo,C., Accadia,M., Lapunzina,P., Cubellis,M.V., de Nanclares,G.P., Monk,D., Riccio,A. and Cerrato,F. TITLE Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances JOURNAL Clin Epigenetics 14 (1), 71 (2022) PUBMED 35643636 REMARK GeneRIF: Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith-Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances. Publication Status: Online-Only REFERENCE 3 (bases 1 to 1037) AUTHORS Fatemi,N., Ray,P.F., Ramezanali,F., Shahani,T., Amiri-Yekta,A., Kherraf,Z.E., Cazin,C., Almadani,N., Varkiani,M., Sarmadi,S., Sodeifi,N., Gourabi,H., Biglari,A. and Totonchi,M. TITLE KH domain containing 3 like (KHDC3L) frame-shift mutation causes both recurrent pregnancy loss and hydatidiform mole JOURNAL Eur J Obstet Gynecol Reprod Biol 259, 100-104 (2021) PUBMED 33639414 REMARK GeneRIF: KH domain containing 3 like (KHDC3L) frame-shift mutation causes both recurrent pregnancy loss and hydatidiform mole. REFERENCE 4 (bases 1 to 1037) AUTHORS Luck,K., Kim,D.K., Lambourne,L., Spirohn,K., Begg,B.E., Bian,W., Brignall,R., Cafarelli,T., Campos-Laborie,F.J., Charloteaux,B., Choi,D., Cote,A.G., Daley,M., Deimling,S., Desbuleux,A., Dricot,A., Gebbia,M., Hardy,M.F., Kishore,N., Knapp,J.J., Kovacs,I.A., Lemmens,I., Mee,M.W., Mellor,J.C., Pollis,C., Pons,C., Richardson,A.D., Schlabach,S., Teeking,B., Yadav,A., Babor,M., Balcha,D., Basha,O., Bowman-Colin,C., Chin,S.F., Choi,S.G., Colabella,C., Coppin,G., D'Amata,C., De Ridder,D., De Rouck,S., Duran-Frigola,M., Ennajdaoui,H., Goebels,F., Goehring,L., Gopal,A., Haddad,G., Hatchi,E., Helmy,M., Jacob,Y., Kassa,Y., Landini,S., Li,R., van Lieshout,N., MacWilliams,A., Markey,D., Paulson,J.N., Rangarajan,S., Rasla,J., Rayhan,A., Rolland,T., San-Miguel,A., Shen,Y., Sheykhkarimli,D., Sheynkman,G.M., Simonovsky,E., Tasan,M., Tejeda,A., Tropepe,V., Twizere,J.C., Wang,Y., Weatheritt,R.J., Weile,J., Xia,Y., Yang,X., Yeger-Lotem,E., Zhong,Q., Aloy,P., Bader,G.D., De Las Rivas,J., Gaudet,S., Hao,T., Rak,J., Tavernier,J., Hill,D.E., Vidal,M., Roth,F.P. and Calderwood,M.A. TITLE A reference map of the human binary protein interactome JOURNAL Nature 580 (7803), 402-408 (2020) PUBMED 32296183 REFERENCE 5 (bases 1 to 1037) AUTHORS Zhang,W., Chen,Z., Zhang,D., Zhao,B., Liu,L., Xie,Z., Yao,Y. and Zheng,P. TITLE KHDC3L mutation causes recurrent pregnancy loss by inducing genomic instability of human early embryonic cells JOURNAL PLoS Biol 17 (10), e3000468 (2019) PUBMED 31609975 REMARK GeneRIF: The study specified KHDC3L as a new recurrent pregnancy loss risk gene, and recognized its critical function in DNA damage repair pathways. Publication Status: Online-Only REFERENCE 6 (bases 1 to 1037) AUTHORS Fallahian,M., Sebire,N.J., Savage,P.M., Seckl,M.J. and Fisher,R.A. TITLE Mutations in NLRP7 and KHDC3L confer a complete hydatidiform mole phenotype on digynic triploid conceptions JOURNAL Hum Mutat 34 (2), 301-308 (2013) PUBMED 23125094 REMARK GeneRIF: Both NLRP7 and KHDC3L are involved in setting or maintaining the appropriate imprint within the ovum in women with familial recurrent hydatidiform mole. REFERENCE 7 (bases 1 to 1037) AUTHORS Andreasen,L., Bolund,L., Niemann,I., Hansen,E.S. and Sunde,L. TITLE Mosaic moles and non-familial biparental moles are not caused by mutations in NLRP7, NLRP2 or C6orf221 JOURNAL Mol Hum Reprod 18 (12), 593-598 (2012) PUBMED 22909446 REMARK GeneRIF: Observations suggest that although NLRP7 and C6orf221 mutations are related to diploid biparental FRHMs, neither of these genes, nor NLRP2, are related to diploid HMs with biparental contributions to the molar genome. REFERENCE 8 (bases 1 to 1037) AUTHORS Parry,D.A., Logan,C.V., Hayward,B.E., Shires,M., Landolsi,H., Diggle,C., Carr,I., Rittore,C., Touitou,I., Philibert,L., Fisher,R.A., Fallahian,M., Huntriss,J.D., Picton,H.M., Malik,S., Taylor,G.R., Johnson,C.A., Bonthron,D.T. and Sheridan,E.G. TITLE Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte JOURNAL Am J Hum Genet 89 (3), 451-458 (2011) PUBMED 21885028 REMARK GeneRIF: Mutations causing familial biparental hydatidiform mole implicate c6orf221 as a possible regulator of genomic imprinting in the human oocyte. REFERENCE 9 (bases 1 to 1037) AUTHORS Pierre,A., Gautier,M., Callebaut,I., Bontoux,M., Jeanpierre,E., Pontarotti,P. and Monget,P. TITLE Atypical structure and phylogenomic evolution of the new eutherian oocyte- and embryo-expressed KHDC1/DPPA5/ECAT1/OOEP gene family JOURNAL Genomics 90 (5), 583-594 (2007) PUBMED 17913455 REMARK GeneRIF: This paper states that ECAT1 is not found in rodents. REFERENCE 10 (bases 1 to 1037) AUTHORS Mitsui,K., Tokuzawa,Y., Itoh,H., Segawa,K., Murakami,M., Takahashi,K., Maruyama,M., Maeda,M. and Yamanaka,S. TITLE The homeoprotein Nanog is required for maintenance of pluripotency in mouse epiblast and ES cells JOURNAL Cell 113 (5), 631-642 (2003) PUBMED 12787504 COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The reference sequence was derived from AC019205.4, AB211062.1 and AI638315.1. This sequence is a reference standard in the RefSeqGene project. On Nov 23, 2018 this sequence version replaced NM_001017361.2. Summary: The protein encoded by this gene belongs to the KHDC1 family, members of which contain an atypical KH domain that may not bind RNA like canonical KH domains. This gene is specifically expressed in the oocytes, and recent studies suggest that it may function as a regulator of genomic imprinting in the oocyte. Mutations in this gene are associated with recurrent biparental complete hydatidiform mole. [provided by RefSeq, Dec 2011]. 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 :: AB211062.1, BC132844.1 [ECO:0000332] RNAseq introns :: single sample supports all introns SAMEA1968968, SAMEA2142363 [ECO:0000348] ##Evidence-Data-END## ##RefSeq-Attributes-START## MANE Ensembl match :: ENST00000370367.4/ ENSP00000359392.3 RefSeq Select criteria :: based on single protein-coding transcript ##RefSeq-Attributes-END## COMPLETENESS: full length. PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-19 AC019205.4 80885-80903 c 20-904 AB211062.1 1-885 905-1037 AI638315.1 10-142 c FEATURES Location/Qualifiers source 1..1037 /organism="Homo sapiens" /mol_type="mRNA" /db_xref="taxon:9606" /chromosome="6" /map="6q13" gene 1..1037 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /note="KH domain containing 3 like, subcortical maternal complex member" /db_xref="GeneID:154288" /db_xref="HGNC:HGNC:33699" /db_xref="MIM:611687" exon 1..241 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /inference="alignment:Splign:2.1.0" variation 1 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768884233" variation 2 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768884278" variation 3 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:1305069572" variation 5 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:535114156" variation 6 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1768884450" variation 7 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768884499" variation 9 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:954877750" variation 10 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:778501993" variation 13 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768884693" variation 17 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1022527171" variation 18..19 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="gc" /replace="gcgc" /db_xref="dbSNP:1768884807" variation 22 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1400417344" variation 28 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:368756507" variation 29 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:770253703" variation 30 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1192756306" variation 31 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1562274416" variation 32 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1476901753" variation 37 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:773337596" variation 39 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:1267870291" variation 40 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1411888708" variation 41 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1421014012" variation 43 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1194329671" variation 45 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768885445" variation 49 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1019814442" variation 53 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:999795233" variation 55 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1582618908" variation 56 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1562274427" variation 58 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="aa" /db_xref="dbSNP:1562274429" variation 59 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1214452457" variation 60 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1312466796" variation 61 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1582618914" variation 62 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1363771323" variation 63 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768886006" variation 64 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:371916561" variation 67 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1315216321" variation 68 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:766529626" CDS 73..726 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /note="ES cell-associated transcript 1 protein; KHDC3-like protein" /codon_start=1 /product="KH domain-containing protein 3" /protein_id="NP_001017361.1" /db_xref="CCDS:CCDS34484.1" /db_xref="GeneID:154288" /db_xref="HGNC:HGNC:33699" /db_xref="MIM:611687" /translation="
MDAPRRFPTLVQLMQPKAMPVEVLGHLPKRFSWFHSEFLKNPKVVRLEVWLVEKIFGRGGERIPHVQGMSQILIHVNRLDPNGEAEILVFGRPSYQEDTIKMIMNLADYHRQLQAKGSGKALAQDVATQKAETQRSSIEVREAGTQRSVEVREAGTQRSVEVQEVGTQGSPVEVQEAGTQQSLQAANKSGTQRSPEAASKAVTQRFREDARDPVTRL"
misc_feature 73..192 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /note="propagated from UniProtKB/Swiss-Prot (Q587J8.1); Region: Involved in RNA binding. /evidence=ECO:0000250|UniProtKB:Q9CWU5" misc_feature 157..408 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /note="KH-like RNA-binding domain; Region: MOEP19; pfam16005" /db_xref="CDD:464969" misc_feature 457..723 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /note="propagated from UniProtKB/Swiss-Prot (Q587J8.1); Region: Disordered. /evidence=ECO:0000256|SAM:MobiDB-lite" misc_feature 505..507 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /note="Phosphothreonine, by ATM. /evidence=ECO:0000269|PubMed:31609975; propagated from UniProtKB/Swiss-Prot (Q587J8.1); phosphorylation site" misc_feature 538..540 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /note="Phosphothreonine, by ATM. /evidence=ECO:0000269|PubMed:31609975; propagated from UniProtKB/Swiss-Prot (Q587J8.1); phosphorylation site" misc_feature 616..618 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /note="Phosphoserine. /evidence=ECO:0000250|UniProtKB:Q9CWU5; propagated from UniProtKB/Swiss-Prot (Q587J8.1); phosphorylation site" variation 73 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:606231235" variation 74 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:774559307" variation 75 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:606231233" variation 78 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1376501368" variation 79 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:879587586" variation 80 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:149498621" variation 82 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:763895578" variation 83 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:968324083" variation 85 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:753622103" variation 86 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:144291287" variation 87 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:192258859" variation 88..109 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="cggtttccgacgctcgtgcaac" /db_xref="dbSNP:1768887476" variation 88 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:369951888" variation 89 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1235991286" variation 91 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:75347618" variation 95 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:757863032" variation 96 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:148734762" variation 98 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1249850571" variation 99 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:751290906" variation 101 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:953883035" variation 102 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1260917217" variation 103..111 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="gtgcaactg" /replace="gtgcaactggtgcaactg" /db_xref="dbSNP:767338149" variation 103 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:372943893" variation 106 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1434551745" variation 112 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:781673395" variation 113 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1768888383" variation 120 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1221868722" variation 121 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:992667093" variation 123 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1238657557" variation 127 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:916019714" variation 130 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1322317733" variation 132 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1457652305" variation 136 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1443861825" variation 138 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:748502124" variation 140 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1582619034" variation 145 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:770321628" variation 149 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:778156260" variation 152 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:749321389" variation 153 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:759991776" variation 155 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:948834870" variation 158 /gene="KHDC3L" /gene_synonym="C6orf221; 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ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:768132139" exon 422..1037 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /inference="alignment:Splign:2.1.0" variation 423 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1489820494" variation 428 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1768907307" variation 430 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:769070031" variation 433 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1267639775" variation 438 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:933529284" variation 440 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1384312110" variation 443 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:546109354" variation 445 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:140227556" variation 447 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:1582619686" variation 448 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1768907518" variation 454 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:902646106" variation 455 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:368968805" variation 456 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1222808642" variation 458 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:145650848" variation 460 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:761435959" variation 466 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1487310284" variation 470 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:151102141" variation 471 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:773563196" variation 472 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:763433087" variation 474 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:564440304" variation 475 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:531383488" variation 476 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1488094962" variation 477 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1768908147" variation 478..515 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="tc" /replace="tcttcaatagaagtccgggaggccgggacgcagcgttc" /db_xref="dbSNP:1191856901" variation 478 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:759484258" variation 479 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1302690286" variation 482 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:779270209" variation 483 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:549971311" variation 484 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:752863062" variation 485 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:756397634" variation 487 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1022599477" variation 488 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1768908508" variation 490..539 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="gtccgggaggccgggac" /replace="gtccgggaggccgggacgcagcgttcggtggaggtccgggaggccggg ac" /replace="gtccgggaggccgggacgcagcgttcggtggaggtccgggaggccggg acgcagcgttcggtggaggtccgggaggccgggac" /db_xref="dbSNP:1384034779" variation 490 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:561595924" variation 491 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1562274861" variation 492..505 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="ccggga" /replace="ccgggaggccggga" /db_xref="dbSNP:753925032" variation 494 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1455756972" variation 495 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1426953758" variation 496 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:143527822" variation 497 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:778196357" variation 499 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:750124331" variation 501 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:758213353" variation 502 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1296027463" variation 503 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1356955555" variation 504 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:779819678" variation 506 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768909125" variation 507 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1178317016" variation 508..554 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="cagcgttcggtgga" /replace="cagcgttcggtggaggtccgggaggccgggacccagcgttcggtgga" /replace="cagcgttcggtggaggtccgggaggccgggacccagcgttcggtggag gtccgggaggccgggacccagcgttcggtgga" /db_xref="dbSNP:755542796" variation 509 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:970134596" variation 510 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1768909293" variation 511 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:746993238" variation 511 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="cc" /db_xref="dbSNP:1311338803" variation 512 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1768909332" variation 515 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1241027501" variation 516 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:2150775969" variation 518 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1562274879" variation 519..520 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="gg" /replace="ggg" /db_xref="dbSNP:1562274883" variation 519 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:780652763" variation 520 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:267601110" variation 522 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1486578798" variation 523..545 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="gtccgggaggccgggacccagcg" /replace="gtccgggaggccgggacccagcggtcttcaatagaagtccgggaggcc gggacccagcg" /db_xref="dbSNP:1562274891" variation 523..539 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="gtccgggaggccgggac" /replace="gtccgggaggccgggacgcagcgttcggtggaagtccgggaggccggg ac" /db_xref="dbSNP:1562274888" variation 523 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1768909616" variation 526 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768909745" variation 527 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:867183004" variation 528..613 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="ggaggccgggacccagc" /replace="ggaggccgggacccagcgttcggtggaagtccaggaggtcgggacaca gggttctccggtggaggtgcaggaggccgggacccagc" /db_xref="dbSNP:1562274898" variation 528..565 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="ggagg" /replace="ggaggccgggacccagcgttcggtggaagtccaggagg" /db_xref="dbSNP:1768909951" variation 528 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1415006512" variation 531 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1352786998" variation 532 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1214149229" variation 533 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1768910136" variation 534..572 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="cgggac" /replace="cgggacccagcgttcggtggaagtccaggaggtcgggac" /db_xref="dbSNP:1214649224" variation 534 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:747724589" variation 535 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:769425065" variation 537 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1768910320" variation 538 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="aa" /db_xref="dbSNP:779501573" variation 538 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:367829712" variation 540 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:139884562" variation 541 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768910571" variation 544 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1721782869" variation 545 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1159857446" variation 546 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768910655" variation 548 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:771348060" variation 549 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:993890975" variation 555 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:546943857" variation 558 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:149813497" variation 559..601 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="caggaggtcgggacacagggttctccggtggaggtgcaggagg" /replace="caggaggtcgggacacagggttctccggtggaggtgcaggaggtcggg acacagggttctccggtggaggtgcaggagg" /db_xref="dbSNP:753246137" variation 560 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:768202601" variation 564 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:775695947" variation 566 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1430362385" variation 567 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:372017888" variation 569 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:764341899" variation 570 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1768911173" variation 572 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1466187951" variation 573 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1768911262" variation 575 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:754125013" variation 577 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:758082018" variation 578 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:766179045" variation 579 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1309945219" variation 580 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1562274929" variation 582 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:1768911546" variation 583 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1420968441" variation 584 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:376952167" variation 585 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1376020646" variation 588 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:983603657" variation 591 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:368252944" variation 594 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:565335780" variation 595 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:747602045" variation 596 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:200454909" variation 598 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1254478088" variation 600 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:912085147" variation 601 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:755627817" variation 602 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1179315654" variation 603 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:61746688" variation 604 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:748946658" variation 606 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:140872763" variation 608 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:921916889" variation 609 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:774772638" variation 612 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:61746689" variation 613 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:772644928" variation 614 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:1174999673" variation 619 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1357049411" variation 621 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1768913020" variation 623 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:776143413" variation 624 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:760793883" variation 626 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1399480123" variation 629 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1768913203" variation 632 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:764295033" variation 634 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:2150776038" variation 636 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:776626414" variation 637 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1768913337" variation 638 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:868642236" variation 639 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:144624088" variation 640 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:925285023" variation 641 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1218416698" variation 642 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1768913583" variation 644 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:146663357" variation 645 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1309455824" variation 646 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1463521938" variation 647 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:2150776053" variation 649 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1199389748" variation 652 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:1352672567" variation 653 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1257451545" variation 654 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:754781306" variation 655 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:200036428" variation 657 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:367677172" variation 659 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1477932850" variation 661 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1386511019" variation 663 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:756091222" variation 665 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1181386957" variation 667 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:924015567" variation 668 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1422658659" variation 670 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1478569813" variation 672 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:555935608" variation 674 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:561930" variation 680 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1768914817" variation 681 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1250095769" variation 684 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1422197973" variation 685 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:756918113" variation 686 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:373443240" variation 687 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:2150776085" variation 691 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:866082650" variation 692 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1768915292" variation 693 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1768915338" variation 694 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1350378111" variation 697 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1768915420" variation 699 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:553544698" variation 702 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:780661477" variation 703 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:578059080" variation 704 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:545413359" variation 705 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:776772428" variation 708..709 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="" /replace="t" /db_xref="dbSNP:1768915768" variation 708 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:761858437" variation 711..728 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="ag" /replace="agttactagattatgaag" /db_xref="dbSNP:1768915857" variation 711 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1235200861" variation 712 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:61740617" variation 714 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:770000920" variation 714 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="t" /replace="tgtctttctctgtgt" /db_xref="dbSNP:1562275035" variation 715..716 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="" /replace="atacccac" /db_xref="dbSNP:1562275042" variation 715 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:376848709" variation 717 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:2150776100" variation 718 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:143606304" variation 720 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:1768916182" variation 721 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:1044705578" variation 724 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:202161970" variation 728 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1489067451" variation 729 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:760602354" variation 730 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:763995195" variation 731 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:371374179" variation 734 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1768916403" variation 738 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:756721283" variation 741 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1414490653" variation 746 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:778586031" variation 747 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:750119584" variation 748 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:758177277" variation 753 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1768916603" variation 754 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1405421289" variation 758 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1400379268" variation 759 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1297884288" variation 760..763 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="ggg" /replace="gggg" /db_xref="dbSNP:1403276894" variation 760 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:201481971" variation 761 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:747449780" variation 763 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1004649367" variation 766 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1356276799" variation 769 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1227035080" variation 770 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:1286945502" variation 771 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:181090656" variation 777 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1423671842" variation 778 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1216313331" variation 779 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1768917123" variation 786 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768917160" variation 787 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:2150776130" variation 788 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:529101981" variation 789 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1019090995" variation 795 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:966614027" variation 797 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:896303659" variation 799 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:2150776137" variation 802 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:1768917943" variation 803 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1248803984" variation 806 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1023958549" variation 807 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1490636395" variation 809 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1271218943" variation 811 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:2150776142" variation 812 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1582620079" variation 820..825 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="tttttt" /replace="ttttttt" /db_xref="dbSNP:1220328501" variation 823 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:969302554" variation 827 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768918232" variation 830 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1261499095" variation 834 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768918315" variation 835 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1000800174" variation 838 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:3195684" variation 839 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="" /replace="t" /db_xref="dbSNP:1314925598" variation 839 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768918449" variation 845 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1305944853" variation 851 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1417733121" variation 855 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1224119738" variation 857 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1768918613" variation 862 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1768918648" variation 863 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768918687" variation 868 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1768918726" variation 871..876 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="taa" /replace="taataa" /db_xref="dbSNP:1411311999" regulatory 872..877 /regulatory_class="polyA_signal_sequence" /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /note="hexamer: AATAAA" variation 873 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:974978728" variation 878 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1347308827" variation 881 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768918865" variation 883 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1768918934" variation 885 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1032302298" variation 889 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768919017" variation 890 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1300804551" variation 892..893 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="aa" /db_xref="dbSNP:1768919078" polyA_site 893 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" variation 898 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:1403769957" variation 899..920 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="ccccccgcctc" /replace="ccccccgcctcccccccgcctc" /replace="ccccccgcctcccccccgcctcccccccgcctc" /db_xref="dbSNP:1290291697" variation 900 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768919241" variation 902 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768919278" variation 904 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:547083599" variation 905 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1029650791" variation 906 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1768919428" variation 908 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1158881307" variation 909..915 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="cccccc" /replace="ccccccc" /replace="cccccccc" /replace="ccccccccc" /db_xref="dbSNP:113486455" variation 909 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:923418459" variation 910 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1449883838" variation 911..922 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="cccccgcctcac" /db_xref="dbSNP:1768919761" variation 911 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768919719" variation 912 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:559059803" variation 913 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:968357637" variation 914 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:979383209" variation 915..916 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="" /replace="t" /db_xref="dbSNP:1562275138" variation 915 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1222774175" variation 916 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1326523366" variation 921 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1768920037" variation 924 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1297011318" variation 925 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:923961619" variation 927 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:955025569" variation 932 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1768920198" variation 937 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /db_xref="dbSNP:1728964162" variation 938 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="t" /replace="tt" /db_xref="dbSNP:1768920244" variation 940 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1768920287" variation 941 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1383770896" variation 943 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768920365" variation 944 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:532735031" variation 945 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1429929912" variation 946 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:910725555" variation 946 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="cc" /db_xref="dbSNP:1768920564" variation 947 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /replace="t" /db_xref="dbSNP:551370250" variation 951 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1268202111" variation 954 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:1204286084" variation 960 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:992210178" variation 962 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1195399870" variation 963 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1768920817" variation 964 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="t" /db_xref="dbSNP:1768920854" variation 965..970 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="tt" /replace="ttgttt" /db_xref="dbSNP:1768920940" variation 965..966 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="t" /replace="tt" /db_xref="dbSNP:1220730811" variation 966..968 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="t" /replace="tgt" /db_xref="dbSNP:1768920974" variation 973 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="" /replace="g" /db_xref="dbSNP:1247612375" variation 973 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="g" /db_xref="dbSNP:1768921007" variation 980 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1204507113" variation 982 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1260962452" variation 985 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1202961776" variation 987 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="g" /replace="t" /db_xref="dbSNP:917048060" variation 988 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:2150776218" variation 991 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1224578892" variation 993 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768921277" variation 994 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1768921308" variation 996 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /replace="t" /db_xref="dbSNP:1325529617" variation 998 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:949919694" variation 1000..1007 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="caacacaa" /replace="caacacaacacaa" /db_xref="dbSNP:919560993" variation 1000 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1385450960" variation 1001..1002 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="aa" /db_xref="dbSNP:1768921486" variation 1004 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="aa" /db_xref="dbSNP:1768921541" variation 1005 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768921584" variation 1006 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1562275168" variation 1011 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="g" /replace="t" /db_xref="dbSNP:1768921657" variation 1012 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1323068498" variation 1013 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="g" /db_xref="dbSNP:1768921738" variation 1018 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768921775" regulatory 1019..1024 /regulatory_class="polyA_signal_sequence" /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /note="hexamer: AATAAA" variation 1019 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1414461181" variation 1028 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:2295761" variation 1031 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="a" /replace="c" /db_xref="dbSNP:1245040997" polyA_site 1037 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /note="major polyA site" variation 1037 /gene="KHDC3L" /gene_synonym="C6orf221; ECAT1; HYDM2" /replace="c" /replace="t" /db_xref="dbSNP:1768921992" ORIGIN
ctagtctcccagctccagctcggcctttgggtttgctgtggtgtccttgtctcctgcaggaccggccgcagcatggacgctcccaggcggtttccgacgctcgtgcaactgatgcagccaaaagcaatgccagtggaggtgctcggtcacctccctaagcggttctcctggttccactctgagttcctgaagaatccgaaggtagttcgccttgaggtttggctggtggaaaagatcttcggccggggcggagaacgcatcccgcacgtccagggtatgtcccaaatcttgattcacgtgaatcgattggaccctaacggcgaggctgagatcttggtatttgggaggccttcttaccaggaggacacaatcaagatgatcatgaacctggctgactatcaccgccagctccaggcgaaaggctcaggaaaggccctcgcccaggatgtcgccactcagaaggccgagacccagcggtcttcaatagaagtccgggaggccgggacgcagcgttcggtggaggtccgggaggccgggacccagcgttcggtggaagtccaggaggtcgggacacagggttctccggtggaggtgcaggaggccgggacccagcagtctctccaggctgccaacaagtcggggacccagcgatcccccgaagctgccagcaaggcagtgacccagcggtttcgcgaggatgcccgggacccagttactagattatgaaggcatctcaggccctggagccagagccagtcaggggttaaagtgaaagcccgtatttccgcccagaagctggggttggggagaggatgtggattttttgttttaccctttctgttgcatggttgcaaacacaaacttgagttctaataaagaattgcaaagtggaagcccgccccccgcctcccccccgcctcacttaagtccaggaagctggggtggcgaggaaggatgatgtggattgtttttgttttacaccttctgttgaatggttgccaacacaaacttgagttctaataaataattgcatttcc
//
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.
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