Variant #0000146070 (NC_000011.9:g.61735061T>A, NM_002032.2:c.-164A>T (FTH1))

Chromosome 11
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.61735061T>A
DNA change (hg38) g.61967589T>A
Published as -
ISCN -
DB-ID FTH1_000001 See all 3 reported entries
Variant remarks variant IRE showed higher binding affinity to IRP
(Kd=13.6 pM) than wild-type (Kd= 30 pM), suppressing H-subunit mRNA translation
Reference PubMed: Kato 2001, Journal: Kato 2001
ClinVar ID -
dbSNP ID rs387906549
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2016-11-25 13:57:43 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FTH1 NM_002032.2 +/. 1 c.-164A>T r.-164a>u p.(=)


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