Variant #0001050675 (NC_000002.11:g.63831834C>T, NM_015910.5:c.-16429G>A (WDPCP))

Chromosome 2
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.63831834C>T
DNA change (hg38) -
Published as MDH1(NM_005917.4):c.503C>T (p.(Ala168Val))
ISCN -
DB-ID MDH1_000008
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) 2.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MDH1 NM_001199111.1 ?/. - c.557C>T r.(?) p.(Ala186Val)
WDPCP NM_015910.5 ?/. - c.-16429G>A r.(?) p.(=)


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