Variant #0005355259 (NC_000007.13:g.150720865C>T, NM_007188.3:c.-4738C>T (ABCB8))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.150720865C>T
DB-ID -
dbSNP ID rs779864415
gnomAD frequency 4/245594
gnomAD homozygote count 0/122793
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     
ABCB8 NM_007188.3 ./. c.-4738C>T r.(=) p.(=)
ATG9B NM_173681.5 ./. c.551-48G>A r.(=) p.(=)