Variant #0000540541 (NC_000010.10:g.71136821C>A, NM_000188.2:c.1007C>A (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.71136821C>A
DNA change (hg38) g.69377065C>A
Published as HK1(NM_033500.2):c.971C>A (p.T324N)
ISCN -
DB-ID HK1_000049
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HK1 NM_000188.2 ?/. - c.1007C>A r.(?) p.(Thr336Asn)
HK1 NM_033500.2 ?/. - c.971C>A r.(?) p.(Thr324Asn)


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