Variant #0000971688 (NC_000010.10:g.71142311C>T, NM_000188.2:c.1334C>T (HK1))

Chromosome 10
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.71142311C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID HK1_000050 See all 6 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1064794848
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-03-12 09:23:01 +01:00 (CET)
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.1334C>T r.(?) p.(Ser445Leu)


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