Variant #0007642387 (NC_000011.9:g.119020733A>T, NM_001142505.1:c.58A>T (ABCG4))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.119020733A>T
DB-ID -
dbSNP ID rs765996611
gnomAD frequency 1/244976
gnomAD homozygote count 0/122485
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.58A>T r.(?) p.(Met20Leu)
ABCG4 NM_022169.4 ./. c.58A>T r.(?) p.(Met20Leu)