Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g01320 | A09 | 969697 | C | T | downstream_gene_variant | MODIFIER | c.*3631G>A| |
S219 |
2 | BAA09g01320 | A09 | 970219 | G | A | downstream_gene_variant | MODIFIER | c.*3109C>T| |
S107 |
3 | BAA09g01320 | A09 | 970864 | G | A | downstream_gene_variant | MODIFIER | c.*2464C>T| |
S192 |
4 | BAA09g01320 | A09 | 970924 | G | A | downstream_gene_variant | MODIFIER | c.*2404C>T| |
S126 |
5 | BAA09g01320 | A09 | 971780 | G | A | downstream_gene_variant | MODIFIER | c.*1548C>T| |
S203 |
6 | BAA09g01320 | A09 | 971865 | C | T | downstream_gene_variant | MODIFIER | c.*1463G>A| |
S269 |
7 | BAA09g01320 | A09 | 973248 | G | A | downstream_gene_variant | MODIFIER | c.*80C>T| |
S187 |
8 | BAA09g01320 | A09 | 974137 | C | T | intron_variant | MODIFIER | c.470+106G>A| |
S191 |
9 | BAA09g01320 | A09 | 974379 | C | T | missense_variant | MODERATE | c.334G>A|p.Asp112Asn |
S292 |
10 | BAA09g01320 | A09 | 974475 | C | T | missense_variant | MODERATE | c.238G>A|p.Gly80Arg |
S181 |
11 | BAA09g01320 | A09 | 974841 | G | A | upstream_gene_variant | MODIFIER | c.-129C>T| |
S228 |
12 | BAA09g01320 | A09 | 975422 | G | A | upstream_gene_variant | MODIFIER | c.-710C>T| |
S218 |
13 | BAA09g01320 | A09 | 976960 | C | T | upstream_gene_variant | MODIFIER | c.-2248G>A| |
S256 |
14 | BAA09g01320 | A09 | 977411 | G | A | upstream_gene_variant | MODIFIER | c.-2699C>T| |
S184 |
15 | BAA09g01320 | A09 | 977487 | G | A | upstream_gene_variant | MODIFIER | c.-2775C>T| |
S295 |
16 | BAA09g01320 | A09 | 978028 | C | T | upstream_gene_variant | MODIFIER | c.-3316G>A| |
S171 |
17 | BAA09g01320 | A09 | 978154 | G | A | upstream_gene_variant | MODIFIER | c.-3442C>T| |
S252 |