Variant #0001499092 (NC_000002.11:g.44065081G>T, NM_022437.2:c.-1112G>T (ABCG8))

Chromosome 2
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.44065081G>T
DB-ID -
dbSNP ID rs372772883
gnomAD frequency 0/246246
gnomAD homozygote count 0/123122
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     
ABCG5 NM_022436.2 ./. c.157C>A r.(?) p.(Pro53Thr)
ABCG8 NM_022437.2 ./. c.-1112G>T r.(=) p.(=)