Variant #0005045317 (NC_000007.13:g.87032613A>C, NM_018849.2:c.3508-16delTinsG (ABCB4))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.87032613A>C
DB-ID -
dbSNP ID rs31653
gnomAD frequency 1/246112
gnomAD homozygote count 0/2466
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     
ABCB4 NM_000443.3 ./. c.3487-16delTinsG r.(=) p.(=)
CROT NM_001143935.1 ./. c.*4653A>C r.(=) p.(=)
ABCB4 NM_018849.2 ./. c.3508-16delTinsG r.(=) p.(=)
ABCB4 NM_018850.2 ./. c.3346-16delTinsG r.(=) p.(=)
CROT NM_021151.3 ./. c.*4653A>C r.(=) p.(=)