Variant #0007642414 (NC_000011.9:g.119020858C>T, NM_001142505.1:c.183C>T (ABCG4))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.119020858C>T
DB-ID -
dbSNP ID rs139736013
gnomAD frequency 404/246176
gnomAD homozygote count 0/122684
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.183C>T r.(?) p.(Ile61=)
ABCG4 NM_022169.4 ./. c.183C>T r.(?) p.(Ile61=)