Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g16010 | A07 | 22988741 | C | T | missense_variant | MODERATE | c.386C>T|p.Pro129Leu |
S301 |
2 | BAA07g16010 | A07 | 22988992 | G | A | missense_variant | MODERATE | c.637G>A|p.Asp213Asn |
S82 S92 |
3 | BAA07g16010 | A07 | 22989760 | C | T | missense_variant | MODERATE | c.1405C>T|p.Pro469Ser |
S281 |
4 | BAA07g16010 | A07 | 22989920 | C | T | missense_variant | MODERATE | c.1565C>T|p.Thr522Ile |
S75 S81 |
5 | BAA07g16010 | A07 | 22989929 | C | T | missense_variant | MODERATE | c.1574C>T|p.Ala525Val |
S168 |
6 | BAA07g16010 | A07 | 22990090 | G | A | missense_variant | MODERATE | c.1735G>A|p.Ala579Thr |
S61 |
7 | BAA07g16010 | A07 | 22990187 | C | T | missense_variant | MODERATE | c.1832C>T|p.Thr611Met |
S232 |
8 | BAA07g16010 | A07 | 22990415 | G | A | missense_variant | MODERATE | c.2060G>A|p.Gly687Glu |
S193 |