Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g05230 | A09 | 3019340 | C | T | upstream_gene_variant | MODIFIER | c.-2426C>T| |
S269 |
2 | BAA09g05230 | A09 | 3020887 | C | T | upstream_gene_variant | MODIFIER | c.-879C>T| |
S286 |
3 | BAA09g05230 | A09 | 3021030 | C | T | upstream_gene_variant | MODIFIER | c.-736C>T| |
S111 |
4 | BAA09g05230 | A09 | 3021340 | C | T | upstream_gene_variant | MODIFIER | c.-426C>T| |
S151 |
5 | BAA09g05230 | A09 | 3021591 | G | A | upstream_gene_variant | MODIFIER | c.-175G>A| |
S36 |
6 | BAA09g05230 | A09 | 3021947 | T | C | missense_variant | MODERATE | c.182T>C|p.Ile61Thr |
S2 |
7 | BAA09g05230 | A09 | 3022904 | C | T | missense_variant | MODERATE | c.1139C>T|p.Thr380Ile |
S117 |
8 | BAA09g05230 | A09 | 3022994 | C | T | missense_variant | MODERATE | c.1229C>T|p.Ser410Phe |
S43 |
9 | BAA09g05230 | A09 | 3023809 | C | T | missense_variant | MODERATE | c.2044C>T|p.Leu682Phe |
S257 |
10 | BAA09g05230 | A09 | 3024460 | A | C | missense_variant | MODERATE | c.2695A>C|p.Met899Leu |
S283 S298 S61 S65 |
11 | BAA09g05230 | A09 | 3025944 | C | T | downstream_gene_variant | MODIFIER | c.*1047C>T| |
S37 |