Genomic variant #0000587507

Individual ID 00000003
Chromosome 12
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.53309237G>A
Reference dbSNP
DB-ID AAAS_000010
Frequency 0.948
Allele Count 201
Allele Number 212
Depth 1700
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
AAAS NM_001173466.1 ./.
AAAS NM_015665.5 ./.
AAAS XM_006719617.2 ./.
AAAS XM_006719619.2 ./.
AAAS XM_011538777.1 ./.
AAAS XM_011538778.1 ./.
AAAS XM_011538779.1 ./.
AAAS XM_011538780.1 ./.
AAAS XM_011538781.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin