Variant #0004387942 (NC_000006.11:g.43395815G>C, NM_033450.2:c.-4033G>C (ABCC10))

Chromosome 6
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.43395815G>C
DB-ID -
dbSNP ID rs763991441
gnomAD frequency 1/168598
gnomAD homozygote count 0/84298
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.99G>C r.(?) p.(Val33=)
ABCC10 NM_033450.2 ./. c.-4033G>C r.(=) p.(=)