Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g67070 | A09 | 60966010 | C | T | missense_variant | MODERATE | c.28C>T|p.His10Tyr |
S146 |
2 | BAA09g67070 | A09 | 60966981 | G | A | synonymous_variant | LOW | c.486G>A|p.Glu162Glu |
S208 S93 |
3 | BAA09g67070 | A09 | 60967104 | C | T | missense_variant | MODERATE | c.533C>T|p.Pro178Leu |
S259 |
4 | BAA09g67070 | A09 | 60967212 | G | A | missense_variant | MODERATE | c.641G>A|p.Gly214Glu |
S115 |
5 | BAA09g67070 | A09 | 60967349 | C | T | missense_variant | MODERATE | c.691C>T|p.Leu231Phe |
S38 |
6 | BAA09g67070 | A09 | 60968543 | G | A | missense_variant | MODERATE | c.1501G>A|p.Glu501Lys |
S116 |
7 | BAA09g67070 | A09 | 60968736 | C | T | missense_variant | MODERATE | c.1694C>T|p.Thr565Ile |
S241 |
8 | BAA09g67070 | A09 | 60968925 | G | A | missense_variant | MODERATE | c.1804G>A|p.Ala602Thr |
S8 |
9 | BAA09g67070 | A09 | 60968976 | G | A | missense_variant | MODERATE | c.1855G>A|p.Glu619Lys |
S164 |
10 | BAA09g67070 | A09 | 60969121 | G | A | missense_variant | MODERATE | c.2000G>A|p.Gly667Glu |
S216 |
11 | BAA09g67070 | A09 | 60973224 | C | T | downstream_gene_variant | MODIFIER | c.*2091C>T| |
S217 |
12 | BAA09g67070 | A09 | 60974637 | C | T | downstream_gene_variant | MODIFIER | c.*3504C>T| |
S149 |
13 | BAA09g67070 | A09 | 60975039 | C | T | downstream_gene_variant | MODIFIER | c.*3906C>T| |
S37 |
14 | BAA09g67070 | A09 | 60975052 | C | T | downstream_gene_variant | MODIFIER | c.*3919C>T| |
S65 |