Genomic variant #0000848143

Individual ID 00000001
Chromosome 12
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.9258821A>G
Reference dbSNP
DB-ID A2M_000005
dbSNP ID rs12427063
Frequency 0.32939
Average frequency (large NGS studies) 0.28934 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Position     

RNA change     

Protein     
A2M NM_000014.4 ./. - c.1104+11T>C - r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA arrayCNV - 904756 Admin