Variant #0007642379 (NC_000011.9:g.119020716G>C, NM_001142505.1:c.41G>C (ABCG4))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.119020716G>C
DB-ID -
dbSNP ID rs760610599
gnomAD frequency 5/243760
gnomAD homozygote count 0/121875
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.41G>C r.(?) p.(Gly14Ala)
ABCG4 NM_022169.4 ./. c.41G>C r.(?) p.(Gly14Ala)