Variant #0000277664 (NC_000010.10:g.71160828C>T, NM_000188.2:c.2691C>T (HK1))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.71160828C>T
DNA change (hg38) g.69401072C>T
Published as HK1(NM_033500.2):c.2655C>T (p.S885=)
ISCN -
DB-ID HK1_000019
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) 0.0223 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-27 14:21:29 +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.2691C>T r.(?) p.(Ser897=)
TACR2 NM_001057.2 -/. - c.*3754G>A r.(=) p.(=)
HK1 NM_033500.2 -/. - c.2655C>T r.(?) p.(Ser885=)


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