Variant #0005048225 (NC_000007.13:g.87339891A>T, NC_000007.13(NM_000927.4):c.-331+2586T>A (ABCB1))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.87339891A>T
DB-ID -
dbSNP ID rs769745143
gnomAD frequency 1/230826
gnomAD homozygote count 0/115412
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     
ABCB1 NM_000927.4 ./. c.-331+2586T>A r.(=) p.(=)
RUNDC3B NM_001134405.1 ./. c.378A>T r.(?) p.(Arg126Ser)
RUNDC3B NM_001134406.1 ./. c.378A>T r.(?) p.(Arg126Ser)
RUNDC3B NM_138290.2 ./. c.429A>T r.(?) p.(Arg143Ser)