Variant #0000616934 (NC_000017.10:g.80405460_80405461del, NM_001033046.3:c.123_124del (C17orf62))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.80405460_80405461del
DNA change (hg38) g.82447584_82447585del
Published as C17orf62(NM_001193653.1):c.123_124delCG (p.S41Rfs*3)
ISCN -
DB-ID C17orf62_000005
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-14 16:09:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C17orf62 NM_001033046.3 +/. - c.123_124del r.(?) p.(Ser41ArgfsTer3)
HEXDC NM_173620.2 +/. - c.*4992_*4993del r.(=) p.(=)
OGFOD3 NM_175902.4 +/. - c.-29099_-29098del r.(?) p.(=)


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