Variant #0001498406 (NC_000002.11:g.44049953G>A, NM_022436.2:c.1446delCinsT (ABCG5))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44049953G>A
DB-ID -
dbSNP ID rs764191918
gnomAD frequency 3/246112
gnomAD homozygote count 0/123052
Average frequency (gnomAD v.2.1.1) 1.0E-5 View details
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     
ABCG5 NM_022436.2 ./. c.1446delCinsT r.(?) p.(Phe482=)