Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g19850 | A05 | 12029757 | G | A | downstream_gene_variant | MODIFIER | c.*4951C>T| |
S144 |
2 | BAA05g19850 | A05 | 12031928 | G | A | downstream_gene_variant | MODIFIER | c.*2780C>T| |
S203 |
3 | BAA05g19850 | A05 | 12032568 | G | A | downstream_gene_variant | MODIFIER | c.*2140C>T| |
S97 |
4 | BAA05g19850 | A05 | 12033233 | C | T | downstream_gene_variant | MODIFIER | c.*1475G>A| |
S174 |
5 | BAA05g19850 | A05 | 12034368 | G | A | downstream_gene_variant | MODIFIER | c.*340C>T| |
S139 |
6 | BAA05g19850 | A05 | 12034663 | C | T | downstream_gene_variant | MODIFIER | c.*45G>A| |
S136 |
7 | BAA05g19850 | A05 | 12035839 | C | T | intron_variant | MODIFIER | c.1049+127G>A| |
S136 |
8 | BAA05g19850 | A05 | 12036967 | G | A | missense_variant | MODERATE | c.326C>T|p.Pro109Leu |
S243 S299 |
9 | BAA05g19850 | A05 | 12037081 | A | C | missense_variant | MODERATE | c.301T>G|p.Leu101Val |
S134 S200 S207 S26 |
10 | BAA05g19850 | A05 | 12038141 | G | A | upstream_gene_variant | MODIFIER | c.-760C>T| |
S138 |
11 | BAA05g19850 | A05 | 12039319 | C | T | upstream_gene_variant | MODIFIER | c.-1938G>A| |
S199 |
12 | BAA05g19850 | A05 | 12039582 | A | G | upstream_gene_variant | MODIFIER | c.-2201T>C| |
S86 |
13 | BAA05g19850 | A05 | 12039929 | G | A | upstream_gene_variant | MODIFIER | c.-2548C>T| |
S161 |
14 | BAA05g19850 | A05 | 12040777 | C | T | upstream_gene_variant | MODIFIER | c.-3396G>A| |
S256 |
15 | BAA05g19850 | A05 | 12040996 | C | T | upstream_gene_variant | MODIFIER | c.-3615G>A| |
S229 |
16 | BAA05g19850 | A05 | 12041283 | G | A | upstream_gene_variant | MODIFIER | c.-3902C>T| |
S132 S137 |
17 | BAA05g19850 | A05 | 12041770 | G | A | upstream_gene_variant | MODIFIER | c.-4389C>T| |
S246 |
18 | BAA05g19850 | A05 | 12041854 | C | T | upstream_gene_variant | MODIFIER | c.-4473G>A| |
S130 |