Variant #0006755970 (NC_000010.10:g.101596022G>C, NM_000392.3:c.3589delGinsC (ABCC2))

Chromosome 10
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.101596022G>C
DB-ID -
dbSNP ID rs768373392
gnomAD frequency 1/246266
gnomAD homozygote count 0/123131
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     
ABCC2 NM_000392.3 ./. c.3589delGinsC r.(?) p.(Val1197Leu)