Variant #0008574273 (NC_000013.10:g.95953485G>A, NC_000013.10(NM_005845.3):c.74+10C>T (ABCC4))

Chromosome 13
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.95953485G>A
DB-ID -
dbSNP ID rs11568682
gnomAD frequency 3929/210576
gnomAD homozygote count 73/101432
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.74+10C>T r.(=) p.(=)
ABCC4 NM_005845.3 ./. c.74+10C>T r.(=) p.(=)