Variant #0005048226 (NC_000007.13:g.87339893C>G, NC_000007.13(NM_000927.4):c.-331+2584G>C (ABCB1))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.87339893C>G
DB-ID -
dbSNP ID rs773095108
gnomAD frequency 1/234800
gnomAD homozygote count 0/117399
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+2584G>C r.(=) p.(=)
RUNDC3B NM_001134405.1 ./. c.380C>G r.(?) p.(Ala127Gly)
RUNDC3B NM_001134406.1 ./. c.380C>G r.(?) p.(Ala127Gly)
RUNDC3B NM_138290.2 ./. c.431C>G r.(?) p.(Ala144Gly)