Variant #0007805695 (NC_000012.11:g.9266183G>C, NC_000012.11(NM_000014.4):c.87-44C>G (A2M))

Chromosome 12
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.9266183G>C
DB-ID -
dbSNP ID rs372331511
gnomAD frequency 30/237072
gnomAD homozygote count 1/118507
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.87-44C>G r.(=) p.(=)