Variant #0007642346 (NC_000011.9:g.119020630T>C, NC_000011.9(NM_001142505.1):c.-12-34T>C (ABCG4))

Chromosome 11
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.119020630T>C
DB-ID -
dbSNP ID rs767408403
gnomAD frequency 2/216942
gnomAD homozygote count 0/108469
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.-12-34T>C r.(=) p.(=)
ABCG4 NM_022169.4 ./. c.-12-34T>C r.(=) p.(=)