Variant #0010680046 (NC_000017.10:g.48745150T>A, NM_003786.3:c.1635+32delTinsA (ABCC3))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48745150T>A
DB-ID -
dbSNP ID rs201806971
gnomAD frequency 2/244942
gnomAD homozygote count 0/122456
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     
ABCC3 NM_001144070.1 ./. c.1667delTinsA r.(?) p.(Leu556His)
ABCC3 NM_003786.3 ./. c.1635+32delTinsA r.(=) p.(=)