Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26290 | A09 | 17065877 | G | A | synonymous_variant | LOW | c.3732C>T|p.Val1244Val |
S28 |
2 | BAA09g26290 | A09 | 17066136 | C | T | stop_gained | HIGH | c.3567G>A|p.Trp1189* |
S245 |
3 | BAA09g26290 | A09 | 17067128 | C | T | synonymous_variant | LOW | c.2850G>A|p.Gln950Gln |
S305 |
4 | BAA09g26290 | A09 | 17067761 | G | A | missense_variant | MODERATE | c.2504C>T|p.Ala835Val |
S18 |
5 | BAA09g26290 | A09 | 17069070 | G | A | synonymous_variant | LOW | c.2041C>T|p.Leu681Leu |
S184 |
6 | BAA09g26290 | A09 | 17070023 | C | T | missense_variant | MODERATE | c.1469G>A|p.Gly490Glu |
S28 |
7 | BAA09g26290 | A09 | 17070027 | C | T | missense_variant | MODERATE | c.1465G>A|p.Gly489Ser |
S247 |
8 | BAA09g26290 | A09 | 17071163 | C | T | missense_variant | MODERATE | c.706G>A|p.Glu236Lys |
S208 S93 |
9 | BAA09g26290 | A09 | 17072035 | G | A | missense_variant | MODERATE | c.479C>T|p.Pro160Leu |
S47 |
10 | BAA09g26290 | A09 | 17072618 | G | A | missense_variant | MODERATE | c.113C>T|p.Ala38Val |
S56 |
11 | BAA09g26290 | A09 | 17072791 | G | A | upstream_gene_variant | MODIFIER | c.-61C>T| |
S142 |
12 | BAA09g26290 | A09 | 17073111 | C | T | upstream_gene_variant | MODIFIER | c.-381G>A| |
S182 |
13 | BAA09g26290 | A09 | 17073835 | G | A | upstream_gene_variant | MODIFIER | c.-1105C>T| |
S266 |
14 | BAA09g26290 | A09 | 17074663 | G | A | upstream_gene_variant | MODIFIER | c.-1933C>T| |
S139 |
15 | BAA09g26290 | A09 | 17074789 | C | T | upstream_gene_variant | MODIFIER | c.-2059G>A| |
S187 |
16 | BAA09g26290 | A09 | 17075436 | C | T | upstream_gene_variant | MODIFIER | c.-2706G>A| |
S283 |