Variant #0007804250 (NC_000012.11:g.9223049_9223050insA, NC_000012.11(NM_000014.4):c.4194+34dupT (A2M))

Chromosome 12
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.9223049_9223050insA
DB-ID -
dbSNP ID -
gnomAD frequency 1/232266
gnomAD homozygote count 0/116132
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     
A2M NM_000014.4 ./. c.4194+34dupT r.(=) p.(=)
A2M-AS1 NR_026971.1 ./. n.*2398_*2399insA r.(=) p.(=)