Variant #0007642435 (NC_000011.9:g.119020959T>G, NC_000011.9(NM_001142505.1):c.238+46T>G (ABCG4))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.119020959T>G
DB-ID -
dbSNP ID rs780990886
gnomAD frequency 2/231926
gnomAD homozygote count 0/115961
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     
ABCG4 NM_001142505.1 ./. c.238+46T>G r.(=) p.(=)
ABCG4 NM_022169.4 ./. c.238+46T>G r.(=) p.(=)