Variant #0004387938 (NC_000006.11:g.43395800C>T, NM_033450.2:c.-4048C>T (ABCC10))

Chromosome 6
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43395800C>T
DB-ID -
dbSNP ID rs769986645
gnomAD frequency 2/186898
gnomAD homozygote count 0/93447
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     
ABCC10 NM_001198934.1 ./. c.84C>T r.(?) p.(Cys28=)
ABCC10 NM_033450.2 ./. c.-4048C>T r.(=) p.(=)