Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g23660 | A01 | 12294169 | C | T | missense_variant | MODERATE | c.1324G>A|p.Val442Ile |
S130 |
2 | BAA01g23660 | A01 | 12294171 | C | T | missense_variant | MODERATE | c.1322G>A|p.Arg441Gln |
S69 |
3 | BAA01g23660 | A01 | 12294536 | C | T | synonymous_variant | LOW | c.957G>A|p.Glu319Glu |
S291 |
4 | BAA01g23660 | A01 | 12295179 | G | A | missense_variant | MODERATE | c.314C>T|p.Ala105Val |
S1 S90 |
5 | BAA01g23660 | A01 | 12295226 | C | T | synonymous_variant | LOW | c.267G>A|p.Lys89Lys |
S164 |
6 | BAA01g23660 | A01 | 12296023 | G | A | upstream_gene_variant | MODIFIER | c.-531C>T| |
S268 |
7 | BAA01g23660 | A01 | 12296061 | G | A | upstream_gene_variant | MODIFIER | c.-569C>T| |
S129 |
8 | BAA01g23660 | A01 | 12299491 | G | A | upstream_gene_variant | MODIFIER | c.-3999C>T| |
S129 |
9 | BAA01g23660 | A01 | 12299698 | G | A | upstream_gene_variant | MODIFIER | c.-4206C>T| |
S197 |
10 | BAA01g23660 | A01 | 12299949 | C | T | upstream_gene_variant | MODIFIER | c.-4457G>A| |
S213 |
11 | BAA01g23660 | A01 | 12300215 | G | A | upstream_gene_variant | MODIFIER | c.-4723C>T| |
S28 |
12 | BAA01g23660 | A01 | 12300337 | G | A | upstream_gene_variant | MODIFIER | c.-4845C>T| |
S67 |
13 | BAA01g23660 | A01 | 12300343 | C | T | upstream_gene_variant | MODIFIER | c.-4851G>A| |
S134 S179 S193 S8 |