Variant #0000887364 (NC_000006.11:g.56490058T>C, NM_001723.5:c.3116A>G (DST))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.56490058T>C
DNA change (hg38) g.56625260T>C
Published as DST(NM_001144769.5):c.4628A>G (p.Y1543C)
ISCN -
DB-ID DST_000344
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:01:21 +01:00 (CET)
Date last edited 2026-02-25 18:42:14 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DST NM_001374736.1 ?/. - c.4727A>G r.(?) p.(Tyr1576Cys)
DST NM_001723.5 ?/. - c.3116A>G r.(?) p.(Tyr1039Cys)


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