Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01490 | A02 | 680289 | G | A | missense_variant | MODERATE | c.2456C>T|p.Ser819Phe |
S289 S290 |
2 | BAA02g01490 | A02 | 680358 | C | T | missense_variant | MODERATE | c.2387G>A|p.Gly796Asp |
S246 |
3 | BAA02g01490 | A02 | 680386 | C | T | missense_variant | MODERATE | c.2359G>A|p.Glu787Lys |
S194 |
4 | BAA02g01490 | A02 | 680561 | C | T | synonymous_variant | LOW | c.2184G>A|p.Val728Val |
S6 |
5 | BAA02g01490 | A02 | 680598 | C | T | missense_variant | MODERATE | c.2147G>A|p.Arg716Lys |
S280 |
6 | BAA02g01490 | A02 | 680704 | C | T | missense_variant | MODERATE | c.2041G>A|p.Glu681Lys |
S2 |
7 | BAA02g01490 | A02 | 681055 | C | T | synonymous_variant | LOW | c.1761G>A|p.Glu587Glu |
S167 |
8 | BAA02g01490 | A02 | 681644 | C | T | missense_variant | MODERATE | c.1495G>A|p.Glu499Lys |
S120 |
9 | BAA02g01490 | A02 | 682767 | C | T | missense_variant | MODERATE | c.1009G>A|p.Glu337Lys |
S70 |
10 | BAA02g01490 | A02 | 682817 | G | A | missense_variant | MODERATE | c.959C>T|p.Ala320Val |
S276 |
11 | BAA02g01490 | A02 | 683758 | G | A | missense_variant | MODERATE | c.638C>T|p.Ser213Leu |
S265 |
12 | BAA02g01490 | A02 | 684636 | C | T | synonymous_variant | LOW | c.246G>A|p.Leu82Leu |
S292 |
13 | BAA02g01490 | A02 | 688279 | G | A | upstream_gene_variant | MODIFIER | c.-3186C>T| |
S44 |
14 | BAA02g01490 | A02 | 689474 | G | A | upstream_gene_variant | MODIFIER | c.-4381C>T| |
S173 |