Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38480 | A02 | 32769676 | G | A | synonymous_variant | LOW | c.3465C>T|p.His1155His |
S153 S213 |
2 | BAA02g38480 | A02 | 32770308 | C | T | missense_variant | MODERATE | c.2918G>A|p.Gly973Glu |
S77 S82 |
3 | BAA02g38480 | A02 | 32770597 | G | A | synonymous_variant | LOW | c.2710C>T|p.Leu904Leu |
S251 |
4 | BAA02g38480 | A02 | 32771603 | C | T | missense_variant | MODERATE | c.1967G>A|p.Arg656His |
S61 |
5 | BAA02g38480 | A02 | 32772289 | C | T | missense_variant | MODERATE | c.1444G>A|p.Asp482Asn |
S143 |
6 | BAA02g38480 | A02 | 32772504 | G | A | missense_variant | MODERATE | c.1229C>T|p.Ala410Val |
S279 S82 |
7 | BAA02g38480 | A02 | 32772760 | C | T | missense_variant | MODERATE | c.973G>A|p.Gly325Arg |
S108 |
8 | BAA02g38480 | A02 | 32772833 | C | T | synonymous_variant | LOW | c.900G>A|p.Arg300Arg |
S181 |
9 | BAA02g38480 | A02 | 32774381 | G | A | synonymous_variant | LOW | c.249C>T|p.Arg83Arg |
S84 S93 |
10 | BAA02g38480 | A02 | 32774382 | C | T | missense_variant | MODERATE | c.248G>A|p.Arg83His |
S194 |
11 | BAA02g38480 | A02 | 32779101 | C | T | upstream_gene_variant | MODIFIER | c.-4472G>A| |
S208 S219 |