Variant #0007642381 (NC_000011.9:g.119020719C>T, NM_001142505.1:c.44C>T (ABCG4))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.119020719C>T
DB-ID -
dbSNP ID rs113286118
gnomAD frequency 2266/243838
gnomAD homozygote count 26/119679
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCG4 NM_001142505.1 ./. c.44C>T r.(?) p.(Pro15Leu)
ABCG4 NM_022169.4 ./. c.44C>T r.(?) p.(Pro15Leu)