Genomic variant #0000576562

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.8847911T>C
Reference dbSNP
DB-ID A2ML1_000051
Frequency 0.085
Allele Count 15
Allele Number 176
Depth 232
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
A2ML1 NM_001282424.1 ./.
A2ML1 NM_144670.4 ./.
A2ML1 XM_011520566.1 ./.
A2ML1 XM_011520567.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin