Variant #0000081768 (NC_000023.10:g.74290268C>T, NM_004299.4:c.1300G>A (ABCB7))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.74290268C>T
DNA change (hg38) g.75070433C>T
Published as G1305A, E433K
ISCN -
DB-ID ABCB7_000002 See all 3 reported entries
Variant remarks cloned in yeast ATM1 (Atm1p D398K), reduced cytosolic Fe/S protein maturation
Reference PubMed: Bekri 2000, OMIM:var0002
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP 1
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 2009-02-01 12:53:15 +01:00 (CET)
Date last edited 2020-07-20 15:28:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCB7 NM_004299.4 +?/. 10 c.1300G>A r.(?) p.Glu434Lys


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