Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38450 | A09 | 46290203 | G | A | downstream_gene_variant | MODIFIER | c.*2386C>T| |
S166 |
2 | BAA09g38450 | A09 | 46291331 | G | A | downstream_gene_variant | MODIFIER | c.*1258C>T| |
S142 |
3 | BAA09g38450 | A09 | 46293275 | G | A | missense_variant | MODERATE | c.671C>T|p.Ala224Val |
S16 |
4 | BAA09g38450 | A09 | 46294631 | G | A | missense_variant | MODERATE | c.211C>T|p.His71Tyr |
S265 |
5 | BAA09g38450 | A09 | 46294761 | C | T | splice_region_variant&intron_variant | LOW | c.195+5G>A| |
S151 S153 S157 S166 S236 S257 S262 S263 |
6 | BAA09g38450 | A09 | 46295982 | G | A | upstream_gene_variant | MODIFIER | c.-633C>T| |
S288 |
7 | BAA09g38450 | A09 | 46296054 | C | T | upstream_gene_variant | MODIFIER | c.-705G>A| |
S81 |
8 | BAA09g38450 | A09 | 46296452 | G | A | upstream_gene_variant | MODIFIER | c.-1103C>T| |
S172 S217 |
9 | BAA09g38450 | A09 | 46297214 | G | A | upstream_gene_variant | MODIFIER | c.-1865C>T| |
S217 |
10 | BAA09g38450 | A09 | 46297711 | G | A | upstream_gene_variant | MODIFIER | c.-2362C>T| |
S150 |
11 | BAA09g38450 | A09 | 46297745 | C | T | upstream_gene_variant | MODIFIER | c.-2396G>A| |
S63 |
12 | BAA09g38450 | A09 | 46297874 | C | T | upstream_gene_variant | MODIFIER | c.-2525G>A| |
S303 |