Genomic variant #0000587513

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.53314653T>C
Reference dbSNP
DB-ID AAAS_000016
Frequency 0.033
Allele Count 7
Allele Number 210
Depth 661
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