Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41510 | A02 | 34825066 | C | T | missense_variant | MODERATE | c.427C>T|p.Pro143Ser |
S131 |
2 | BAA02g41510 | A02 | 34825957 | G | A | missense_variant | MODERATE | c.1318G>A|p.Val440Ile |
S96 |
3 | BAA02g41510 | A02 | 34825999 | G | A | missense_variant | MODERATE | c.1360G>A|p.Ala454Thr |
S11 |
4 | BAA02g41510 | A02 | 34826011 | C | T | missense_variant | MODERATE | c.1372C>T|p.Pro458Ser |
S283 |
5 | BAA02g41510 | A02 | 34827002 | G | A | missense_variant&splice_region_variant | MODERATE | c.1825G>A|p.Glu609Lys |
S186 |
6 | BAA02g41510 | A02 | 34827354 | G | A | missense_variant | MODERATE | c.2177G>A|p.Gly726Glu |
S110 |
7 | BAA02g41510 | A02 | 34827707 | G | A | missense_variant | MODERATE | c.2444G>A|p.Ser815Asn |
S136 |
8 | BAA02g41510 | A02 | 34827744 | C | T | synonymous_variant | LOW | c.2481C>T|p.Ile827Ile |
S77 S82 |
9 | BAA02g41510 | A02 | 34828984 | C | T | missense_variant | MODERATE | c.2759C>T|p.Ala920Val |
S139 |
10 | BAA02g41510 | A02 | 34829086 | G | A | missense_variant | MODERATE | c.2861G>A|p.Ser954Asn |
S44 |