Variant #0008574229 (NC_000013.10:g.95899921_95899922insCC, NM_005845.3:c.160_161insGG (ABCC4))

Chromosome 13
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.95899921_95899922insCC
DB-ID -
dbSNP ID -
gnomAD frequency 1/246168
gnomAD homozygote count 0/123083
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     
ABCC4 NM_001105515.1 ./. c.160_161insGG r.(?) p.(Gln54ArgfsTer17)
ABCC4 NM_005845.3 ./. c.160_161insGG r.(?) p.(Gln54ArgfsTer17)