Variant #0005048179 (NC_000007.13:g.87323266C>T, NC_000007.13(NM_000927.4):c.-331+19211G>A (ABCB1))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.87323266C>T
DB-ID -
dbSNP ID rs776822862
gnomAD frequency 1/244176
gnomAD homozygote count 0/122087
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+19211G>A r.(=) p.(=)
RUNDC3B NM_138290.2 ./. c.281C>T r.(?) p.(Pro94Leu)