Genomic variant #0000127906

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.219134116G>A
Reference -
DB-ID AAMP_000023
dbSNP ID rs141898578
Frequency 0.007752
Allele Count 4
Allele Number 516
Combined Depth 2284
Homozygous -
Heterozygote -
Average frequency (large NGS studies) 0.00507 View details
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AAMP NM_001087.3 ./. - c.263C>T r.(?) p.(Ala88Val)



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000001 DNA SEQ-NG-I - 825713 Admin