Variant #0005219303 (NC_000007.13:g.121716611C>T, NM_005763.3:c.2713delGinsA (AASS))

Chromosome 7
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.121716611C>T
DB-ID -
dbSNP ID rs772498344
gnomAD frequency 2/245752
gnomAD homozygote count 0/122870
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     
AASS NM_005763.3 ./. c.2713delGinsA r.(?) p.(Gly905Arg)