Genomic variant #0000127886

Individual ID 00000001
Chromosome 2
Allele Unknown
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.219129289C>T
Reference -
DB-ID AAMP_000003
dbSNP ID rs149502890
Frequency 0.003876
Allele Count 2
Allele Number 516
Combined Depth 8502
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.00177 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AAMP NM_001087.3 ./. - c.1272G>A r.(=) p.(=)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin