Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21640 | A10 | 18957414 | G | A | synonymous_variant | LOW | c.69G>A|p.Lys23Lys |
S109 |
2 | BAA10g21640 | A10 | 18957935 | C | T | missense_variant | MODERATE | c.280C>T|p.Pro94Ser |
S275 |
3 | BAA10g21640 | A10 | 18958450 | C | T | synonymous_variant | LOW | c.502C>T|p.Leu168Leu |
S168 |
4 | BAA10g21640 | A10 | 18958471 | C | T | missense_variant | MODERATE | c.523C>T|p.His175Tyr |
S161 |
5 | BAA10g21640 | A10 | 18958648 | C | T | missense_variant | MODERATE | c.700C>T|p.Leu234Phe |
S40 S49 |
6 | BAA10g21640 | A10 | 18958820 | C | T | missense_variant | MODERATE | c.872C>T|p.Thr291Ile |
S80 |
7 | BAA10g21640 | A10 | 18961500 | C | T | missense_variant | MODERATE | c.3028C>T|p.Pro1010Ser |
S191 |
8 | BAA10g21640 | A10 | 18961503 | C | T | synonymous_variant | LOW | c.3031C>T|p.Leu1011Leu |
S47 |
9 | BAA10g21640 | A10 | 18966062 | G | A | downstream_gene_variant | MODIFIER | c.*3489G>A| |
S207 |