Variant #0000081767 (NC_000023.10:g.74291351A>C, ABCB7(NM_004299.4):c.1203T>G)

Chromosome X
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.74291351A>C
DNA change (hg38) g.75071516A>C
Published as 1200T>G, I400M
ISCN -
DB-ID ABCB7_000001 See all 3 reported entries
Variant remarks cloned in yeast ATM1 (V365M), partial loss of function (reduced growth rate iron limiting conditions)
Reference PubMed: Allikmets 1999, OMIM:var0001
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ABCB7 NM_004299.4 +/. 9 c.1203T>G r.(?) p.Ile401Met