Genomic variant #0000411894

Individual ID 00000003
Chromosome 6
Allele Unknown
Affects function (reported) Not classified
Affects function (concluded) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.44302691A>G
Reference dbSNP
DB-ID AARS2_000008
Frequency 0.004717
Allele Count 1
Allele Number 212
Depth 1115
Average frequency (large NGS studies) Variant not found in online data sets
Owner Admin




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     
AARS2 NM_020745.3 ./.
AARS2 XM_005249245.2 ./.
AARS2 XM_011514764.1 ./.



Screenings


Screening ID

Template

Technique

Genes screened

Variants found

Owner
0000000003 DNA SEQ-NG-I - 624137 Admin