Variant #0001037958 (NC_000010.10:g.71075744C>T, NM_000188.2:c.-2960C>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.71075744C>T
DNA change (hg38) -
Published as HK1(NM_033496.3):c.34C>T (p.(Arg12Ter))
ISCN -
DB-ID HK1_000100 See all 2 reported entries
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 2025-05-05 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     
HK1 NM_000188.2 ?/. - c.-2960C>T r.(?) p.(=)
HK1 NM_033500.2 ?/. - c.27+15127C>T r.(=) p.(=)


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