Variant #0000612590 (NC_000010.10:g.71139822C>T, NM_000188.2:c.1236C>T (HK1))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.71139822C>T
DNA change (hg38) g.69380066C>T
Published as HK1(NM_001322365.1):c.1341C>T (p.V447=), HK1(NM_033500.2):c.1200C>T (p.V400=)
ISCN -
DB-ID HK1_000061 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) 4.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-27 14:20:51 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HK1 NM_000188.2 -?/. - c.1236C>T r.(?) p.(Val412=)
HK1 NM_033500.2 -?/. - c.1200C>T r.(?) p.(Val400=)


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