Variant #0007642399 (NC_000011.9:g.119020777C>T, NM_001142505.1:c.102C>T (ABCG4))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.119020777C>T
DB-ID -
dbSNP ID -
gnomAD frequency 1/246050
gnomAD homozygote count 0/123024
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.102C>T r.(?) p.(Thr34=)
ABCG4 NM_022169.4 ./. c.102C>T r.(?) p.(Thr34=)