Variant #0001065242 (NC_000010.10:g.71119761A>G, NM_000188.2:c.335A>G (HK1))

Chromosome 10
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.71119761A>G
DNA change (hg38) -
Published as HK1(NM_000188.3):c.335A>G (p.(Tyr112Cys))
ISCN -
DB-ID chr10_006571
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HK1 NM_000188.2 ?/. - c.335A>G r.(?) p.(Tyr112Cys)
HK1 NM_033500.2 ?/. - c.299A>G r.(?) p.(Tyr100Cys)


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