Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20840 | A01 | 10269361 | C | T | missense_variant | MODERATE | c.86C>T|p.Ser29Phe |
S170 |
2 | BAA01g20840 | A01 | 10269466 | C | T | missense_variant | MODERATE | c.191C>T|p.Ser64Phe |
S69 |
3 | BAA01g20840 | A01 | 10269531 | G | A | missense_variant | MODERATE | c.256G>A|p.Ala86Thr |
S291 |
4 | BAA01g20840 | A01 | 10269702 | C | T | missense_variant | MODERATE | c.427C>T|p.Pro143Ser |
S146 |
5 | BAA01g20840 | A01 | 10269754 | G | T | missense_variant | MODERATE | c.479G>T|p.Arg160Met |
S4 S6 |
6 | BAA01g20840 | A01 | 10270359 | G | A | missense_variant | MODERATE | c.1084G>A|p.Glu362Lys |
S245 S294 |
7 | BAA01g20840 | A01 | 10270719 | G | A | missense_variant | MODERATE | c.1444G>A|p.Val482Ile |
S203 |
8 | BAA01g20840 | A01 | 10270758 | C | T | missense_variant | MODERATE | c.1483C>T|p.Pro495Ser |
S198 |
9 | BAA01g20840 | A01 | 10271770 | G | A | stop_gained | HIGH | c.2061G>A|p.Trp687* |
S116 |
10 | BAA01g20840 | A01 | 10272141 | C | T | missense_variant | MODERATE | c.2432C>T|p.Ser811Phe |
S247 |
11 | BAA01g20840 | A01 | 10273312 | C | T | missense_variant | MODERATE | c.2848C>T|p.Leu950Phe |
S164 |
12 | BAA01g20840 | A01 | 10273422 | G | A | stop_gained | HIGH | c.2958G>A|p.Trp986* |
S57 |
13 | BAA01g20840 | A01 | 10274186 | C | T | missense_variant | MODERATE | c.3722C>T|p.Thr1241Ile |
S84 S93 |
14 | BAA01g20840 | A01 | 10274386 | C | T | missense_variant | MODERATE | c.3922C>T|p.Pro1308Ser |
S38 |