Variant #0007804231 (NC_000012.11:g.9222420T>C, NC_000012.11(NM_000014.4):c.4195-11A>G (A2M))

Chromosome 12
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.9222420T>C
DB-ID -
dbSNP ID rs776763471
gnomAD frequency 4/245928
gnomAD homozygote count 0/122960
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.4195-11A>G r.(=) p.(=)
A2M-AS1 NR_026971.1 ./. n.*1769T>C r.(=) p.(=)