Variant #0005355220 (NC_000007.13:g.150720637C>T, NM_007188.3:c.-4966C>T (ABCB8))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.150720637C>T
DB-ID -
dbSNP ID rs764727074
gnomAD frequency 1/243346
gnomAD homozygote count 0/121672
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     
ABCB8 NM_007188.3 ./. c.-4966C>T r.(=) p.(=)
ATG9B NM_173681.5 ./. c.595-41G>A r.(=) p.(=)