Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17220 | A02 | 8565700 | G | A | missense_variant | MODERATE | c.766C>T|p.Leu256Phe |
S35 |
2 | BAA02g17220 | A02 | 8565856 | C | T | splice_region_variant&synonymous_variant | LOW | c.705G>A|p.Lys235Lys |
S165 |
3 | BAA02g17220 | A02 | 8566542 | G | A | missense_variant | MODERATE | c.401C>T|p.Ala134Val |
S132 S137 S215 S89 |
4 | BAA02g17220 | A02 | 8567594 | C | T | missense_variant&splice_region_variant | MODERATE | c.112G>A|p.Glu38Lys |
S90 |
5 | BAA02g17220 | A02 | 8567635 | G | A | missense_variant | MODERATE | c.71C>T|p.Ser24Phe |
S210 S225 |
6 | BAA02g17220 | A02 | 8567765 | G | A | synonymous_variant | LOW | c.12C>T|p.Ile4Ile |
S122 |
7 | BAA02g17220 | A02 | 8568220 | C | T | upstream_gene_variant | MODIFIER | c.-444G>A| |
S71 |
8 | BAA02g17220 | A02 | 8568323 | G | A | upstream_gene_variant | MODIFIER | c.-547C>T| |
S174 |
9 | BAA02g17220 | A02 | 8569093 | C | T | upstream_gene_variant | MODIFIER | c.-1317G>A| |
S186 |
10 | BAA02g17220 | A02 | 8569155 | G | A | upstream_gene_variant | MODIFIER | c.-1379C>T| |
S170 |
11 | BAA02g17220 | A02 | 8570205 | G | A | upstream_gene_variant | MODIFIER | c.-2429C>T| |
S129 |
12 | BAA02g17220 | A02 | 8572280 | G | A | upstream_gene_variant | MODIFIER | c.-4504C>T| |
S256 |