Genomic variant #0000411886

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.44301928_44301930del
Reference dbSNP
DB-ID AARS2_000057
Frequency 0.133
Allele Count 28
Allele Number 210
Depth 890
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