Genomic variant #0000411882

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.44301286T>C
Reference dbSNP
DB-ID AARS2_000053
Frequency 0.901
Allele Count 191
Allele Number 212
Depth 10724
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