Variant #0012964475 (NC_000023.10:g.74318870G>A, NM_004299.4:c.363C>T (ABCB7))

Chromosome X
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74318870G>A
DB-ID -
dbSNP ID rs764874346
gnomAD frequency 1/177884
gnomAD homozygote count 0/122334
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB7 NM_001271696.1 ./. c.360C>T r.(?) p.(Ile120=)
ABCB7 NM_001271698.1 ./. c.282C>T r.(?) p.(Ile94=)
ABCB7 NM_004299.4 ./. c.363C>T r.(?) p.(Ile121=)