Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14340 | A10 | 15086390 | C | T | missense_variant | MODERATE | c.94C>T|p.Pro32Ser |
S193 S255 |
2 | BAA10g14340 | A10 | 15086511 | C | T | missense_variant | MODERATE | c.215C>T|p.Ala72Val |
S143 |
3 | BAA10g14340 | A10 | 15087549 | C | T | missense_variant | MODERATE | c.1253C>T|p.Ser418Phe |
S140 |
4 | BAA10g14340 | A10 | 15087758 | C | T | missense_variant | MODERATE | c.1462C>T|p.His488Tyr |
S133 |
5 | BAA10g14340 | A10 | 15088075 | C | T | synonymous_variant | LOW | c.1779C>T|p.Arg593Arg |
S247 |
6 | BAA10g14340 | A10 | 15088344 | C | T | missense_variant | MODERATE | c.2048C>T|p.Pro683Leu |
S86 |
7 | BAA10g14340 | A10 | 15092873 | G | A | downstream_gene_variant | MODIFIER | c.*532G>A| |
S57 |