Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g65390 | A03 | 39647264 | G | A | missense_variant | MODERATE | c.112G>A|p.Gly38Arg |
S183 S198 |
2 | BAA03g65390 | A03 | 39647279 | C | T | missense_variant | MODERATE | c.127C>T|p.Leu43Phe |
S16 |
3 | BAA03g65390 | A03 | 39647288 | G | A | missense_variant | MODERATE | c.136G>A|p.Asp46Asn |
S138 |
4 | BAA03g65390 | A03 | 39647473 | G | A | stop_gained | HIGH | c.321G>A|p.Trp107* |
S206 S26 |
5 | BAA03g65390 | A03 | 39647585 | G | A | missense_variant | MODERATE | c.433G>A|p.Val145Ile |
S148 S53 |
6 | BAA03g65390 | A03 | 39647587 | C | T | synonymous_variant | LOW | c.435C>T|p.Val145Val |
S20 |
7 | BAA03g65390 | A03 | 39649367 | G | A | missense_variant | MODERATE | c.1087G>A|p.Ala363Thr |
S136 |
8 | BAA03g65390 | A03 | 39649947 | C | T | missense_variant | MODERATE | c.1334C>T|p.Ala445Val |
S61 |
9 | BAA03g65390 | A03 | 39650169 | G | A | missense_variant | MODERATE | c.1465G>A|p.Gly489Ser |
S236 |
10 | BAA03g65390 | A03 | 39650711 | G | A | missense_variant | MODERATE | c.1903G>A|p.Val635Ile |
S155 S211 |
11 | BAA03g65390 | A03 | 39650722 | C | T | synonymous_variant | LOW | c.1914C>T|p.Tyr638Tyr |
S47 |