Variant #0012964345 (NC_000023.10:g.74291522C>T, NM_004299.4:c.1036-4delGinsA (ABCB7))

Chromosome X
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.74291522C>T
DB-ID -
dbSNP ID rs779385966
gnomAD frequency 1/131732
gnomAD homozygote count 0/86244
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCB7 NM_001271696.1 ./. c.1033-4delGinsA r.spl? p.?
ABCB7 NM_001271697.1 ./. c.913-4delGinsA r.spl? p.?
ABCB7 NM_001271698.1 ./. c.955-4delGinsA r.spl? p.?
ABCB7 NM_001271699.1 ./. c.916-4delGinsA r.spl? p.?
ABCB7 NM_004299.4 ./. c.1036-4delGinsA r.spl? p.?