Variant #0001042296 (NC_000017.10:g.80394608G>A, NM_001033046.3:c.*7272C>T (C17orf62))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.80394608G>A
DNA change (hg38) -
Published as HEXD(NM_001330542.2):c.697G>A (p.(Gly233Ser))
ISCN -
DB-ID C17orf62_000019
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) 0.0002 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C17orf62 NM_001033046.3 -?/. - c.*7272C>T r.(=) p.(=)
HEXDC NM_173620.2 -?/. - c.697G>A r.(?) p.(Gly233Ser)
OGFOD3 NM_175902.4 -?/. - c.-18247C>T r.(?) p.(=)


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