Genomic variant #0000411939
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.44313285_44313293del |
Reference |
dbSNP |
DB-ID |
AARS2_000050 |
Frequency |
0.004717 |
Allele Count |
1 |
Allele Number |
212 |
Depth |
3144 |
Average frequency (large NGS studies) |
Variant not found in online data sets |
Owner |
Admin |
Variant on transcripts
Screenings
|
|