Variant #0000979100 (NC_000010.10:g.71128310A>T, NM_001358263.1:c.526A>T (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.71128310A>T
DNA change (hg38) g.69368554A>T
Published as HK1(NM_000188.3):c.514A>T (p.T172S)
ISCN -
DB-ID HK1_000105
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited 2026-06-26 19:01:41 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HK1 NM_000188.2 ?/. - c.514A>T r.(?) p.(Thr172Ser)
HK1 NM_001358263.1 ?/. - c.526A>T r.(?) p.(Thr176Ser)


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