Variant #0003299627 (NC_000004.11:g.89036229C>G, NM_004827.2:c.842-19delGinsC (ABCG2))

Chromosome 4
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.89036229C>G
DB-ID -
dbSNP ID rs775209989
gnomAD frequency 2/241716
gnomAD homozygote count 0/120855
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     
ABCG2 NM_001257386.1 ./. c.842-19delGinsC r.(=) p.(=)
ABCG2 NM_004827.2 ./. c.842-19delGinsC r.(=) p.(=)