Variant #0001047438 (NC_000006.11:g.26091703G>T, NM_000410.3:c.502G>T (HFE))

Chromosome 6
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.26091703G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID HFE_000035
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs146519482
Origin Unknown
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 2025-08-18 12:06:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HFE NM_000410.3 +/. - c.502G>T r.(?) p.(Glu168Ter)


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