Variant #0010679283 (NC_000017.10:g.48733182_48733183insGTGTCCCCAGGACTCC, NC_000017.10(NM_003786.3):c.46-11_46-10insGTGTCCCCAGGACTCC (ABCC3))

Chromosome 17
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.48733182_48733183insGTGTCCCCAGGACTCC
DB-ID -
dbSNP ID rs748218315
gnomAD frequency 1/244972
gnomAD homozygote count 0/122485
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.46-11_46-10insGTGTCCCCAGGACTCC r.(?) p.(Asn18ValfsTer114)
ABCC3 NM_003786.3 ./. c.46-11_46-10insGTGTCCCCAGGACTCC r.(?) p.(Asn18ValfsTer114)