Variant #0005048168 (NC_000007.13:g.87323196_87323198del, NC_000007.13(NM_000927.4):c.-331+19279_-331+19281del (ABCB1))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.87323196_87323198del
DB-ID -
dbSNP ID rs772869213
gnomAD frequency 47/235500
gnomAD homozygote count 0/117702
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+19279_-331+19281del r.(=) p.(=)
RUNDC3B NM_138290.2 ./. c.239-28_239-26del r.(=) p.(=)