Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g07000 | A05 | 3421618 | C | T | missense_variant | MODERATE | c.443C>T|p.Ser148Phe |
S13 S131 |
2 | BAA05g07000 | A05 | 3421663 | C | T | missense_variant | MODERATE | c.488C>T|p.Pro163Leu |
S303 |
3 | BAA05g07000 | A05 | 3422029 | C | T | missense_variant | MODERATE | c.854C>T|p.Ser285Phe |
S69 |
4 | BAA05g07000 | A05 | 3422601 | C | T | missense_variant | MODERATE | c.953C>T|p.Ser318Leu |
S251 |
5 | BAA05g07000 | A05 | 3422674 | G | A | synonymous_variant | LOW | c.1026G>A|p.Leu342Leu |
S153 |
6 | BAA05g07000 | A05 | 3422700 | C | T | missense_variant | MODERATE | c.1052C>T|p.Ser351Phe |
S179 S193 |
7 | BAA05g07000 | A05 | 3422732 | C | T | synonymous_variant | LOW | c.1084C>T|p.Leu362Leu |
S262 |
8 | BAA05g07000 | A05 | 3422860 | G | A | synonymous_variant | LOW | c.1212G>A|p.Val404Val |
S210 S225 |
9 | BAA05g07000 | A05 | 3423127 | C | T | synonymous_variant | LOW | c.1479C>T|p.Ala493Ala |
S181 |
10 | BAA05g07000 | A05 | 3423374 | G | A | synonymous_variant | LOW | c.1641G>A|p.Arg547Arg |
S48 |
11 | BAA05g07000 | A05 | 3423557 | G | A | synonymous_variant | LOW | c.1824G>A|p.Arg608Arg |
S299 |
12 | BAA05g07000 | A05 | 3423629 | G | A | synonymous_variant | LOW | c.1896G>A|p.Arg632Arg |
S221 |