Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g35610 | A09 | 43989543 | G | A | downstream_gene_variant | MODIFIER | c.*3468C>T| |
S218 |
2 | BAA09g35610 | A09 | 43990380 | G | A | downstream_gene_variant | MODIFIER | c.*2631C>T| |
S75 S81 |
3 | BAA09g35610 | A09 | 43990773 | G | A | downstream_gene_variant | MODIFIER | c.*2238C>T| |
S291 |
4 | BAA09g35610 | A09 | 43991176 | A | T | downstream_gene_variant | MODIFIER | c.*1835T>A| |
S157 |
5 | BAA09g35610 | A09 | 43991262 | G | A | downstream_gene_variant | MODIFIER | c.*1749C>T| |
S249 |
6 | BAA09g35610 | A09 | 43991511 | C | T | downstream_gene_variant | MODIFIER | c.*1500G>A| |
S138 |
7 | BAA09g35610 | A09 | 43992943 | C | T | downstream_gene_variant | MODIFIER | c.*68G>A| |
S235 |
8 | BAA09g35610 | A09 | 43993324 | C | T | missense_variant | MODERATE | c.2543G>A|p.Arg848Lys |
S247 |
9 | BAA09g35610 | A09 | 43993627 | G | A | missense_variant | MODERATE | c.2240C>T|p.Ala747Val |
S291 |
10 | BAA09g35610 | A09 | 43994592 | G | A | missense_variant | MODERATE | c.1633C>T|p.Pro545Ser |
S221 |
11 | BAA09g35610 | A09 | 43994861 | G | A | missense_variant | MODERATE | c.1448C>T|p.Thr483Ile |
S185 |
12 | BAA09g35610 | A09 | 43995393 | C | T | missense_variant | MODERATE | c.1195G>A|p.Ala399Thr |
S206 S26 |
13 | BAA09g35610 | A09 | 43996414 | C | T | synonymous_variant | LOW | c.174G>A|p.Ser58Ser |
S119 |
14 | BAA09g35610 | A09 | 43997978 | C | T | upstream_gene_variant | MODIFIER | c.-1391G>A| |
S94 |
15 | BAA09g35610 | A09 | 43998009 | C | T | upstream_gene_variant | MODIFIER | c.-1422G>A| |
S58 |