Variant #0009333832 (NC_000015.9:g.67495873C>T, NM_001271885.1:c.543+13delGinsA (AAGAB))

Chromosome 15
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.67495873C>T
DB-ID -
dbSNP ID rs760255012
gnomAD frequency 1/244626
gnomAD homozygote count 0/122311
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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AAGAB NM_001271885.1 ./. c.543+13delGinsA r.(=) p.(=)
AAGAB NM_001271886.1 ./. c.543+13delGinsA r.(=) p.(=)
AAGAB NM_024666.4 ./. c.870+13delGinsA r.(=) p.(=)