Variant #0001499250 (NC_000002.11:g.44066294C>T, NC_000002.11(NM_022437.2):c.63+39C>T (ABCG8))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44066294C>T
DB-ID -
dbSNP ID rs112771276
gnomAD frequency 5/145646
gnomAD homozygote count 0/72808
Average frequency (gnomAD v.2.1.1) 3.0E-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.-476G>A r.(=) p.(=)
ABCG8 NM_022437.2 ./. c.63+39C>T r.(=) p.(=)