Variant #0009334276 (NC_000015.9:g.67546969T>C, NM_001031715.2:c.-266T>C (IQCH))

Chromosome 15
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.67546969T>C
DB-ID -
dbSNP ID rs539301011
gnomAD frequency 7/209990
gnomAD homozygote count 0/104988
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     
IQCH NM_001031715.2 ./. c.-266T>C r.(=) p.(=)
AAGAB NM_001271885.1 ./. c.-255+506A>G r.(=) p.(=)
AAGAB NM_001271886.1 ./. c.-472A>G r.(=) p.(=)
IQCH NM_022784.2 ./. c.-266T>C r.(=) p.(=)
AAGAB NM_024666.4 ./. c.1A>G r.(?) p.(Met1?)