Variant #0005048228 (NC_000007.13:g.87339917A>C, NC_000007.13(NM_000927.4):c.-331+2560T>G (ABCB1))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.87339917A>C
DB-ID -
dbSNP ID rs765989518
gnomAD frequency 2/243872
gnomAD homozygote count 0/121934
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     
ABCB1 NM_000927.4 ./. c.-331+2560T>G r.(=) p.(=)
RUNDC3B NM_001134405.1 ./. c.404A>C r.(?) p.(Glu135Ala)
RUNDC3B NM_001134406.1 ./. c.404A>C r.(?) p.(Glu135Ala)
RUNDC3B NM_138290.2 ./. c.455A>C r.(?) p.(Glu152Ala)