Variant #0000678881 (NC_000010.10:g.71129359C>T, NM_000188.2:c.854C>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.71129359C>T
DNA change (hg38) -
Published as HK1(NM_001322365.1):c.959C>T (p.S320F), HK1(NM_001322365.2):c.959C>T (p.S320F)
ISCN -
DB-ID HK1_000070 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) 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HK1 NM_000188.2 ?/. - c.854C>T r.(?) p.(Ser285Phe)
HK1 NM_033500.2 ?/. - c.818C>T r.(?) p.(Ser273Phe)


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