Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10490 | A10 | 12226063 | G | A | upstream_gene_variant | MODIFIER | c.-2954G>A| |
S251 |
2 | BAA10g10490 | A10 | 12226194 | G | A | upstream_gene_variant | MODIFIER | c.-2823G>A| |
S209 |
3 | BAA10g10490 | A10 | 12226236 | C | T | upstream_gene_variant | MODIFIER | c.-2781C>T| |
S232 |
4 | BAA10g10490 | A10 | 12226781 | G | A | upstream_gene_variant | MODIFIER | c.-2236G>A| |
S202 |
5 | BAA10g10490 | A10 | 12229782 | G | A | intron_variant | MODIFIER | c.187+579G>A| |
S172 |
6 | BAA10g10490 | A10 | 12230872 | C | T | intron_variant | MODIFIER | c.188-61C>T| |
S116 |
7 | BAA10g10490 | A10 | 12230906 | C | T | intron_variant | MODIFIER | c.188-27C>T| |
S84 S93 |
8 | BAA10g10490 | A10 | 12231315 | C | T | intron_variant | MODIFIER | c.368-57C>T| |
S301 S304 |
9 | BAA10g10490 | A10 | 12231733 | G | A | intron_variant | MODIFIER | c.464-104G>A| |
S262 |
10 | BAA10g10490 | A10 | 12231939 | G | A | intron_variant | MODIFIER | c.501+65G>A| |
S223 |
11 | BAA10g10490 | A10 | 12233032 | G | A | downstream_gene_variant | MODIFIER | c.*525G>A| |
S127 |
12 | BAA10g10490 | A10 | 12233460 | C | T | downstream_gene_variant | MODIFIER | c.*953C>T| |
S225 |
13 | BAA10g10490 | A10 | 12234836 | C | T | downstream_gene_variant | MODIFIER | c.*2329C>T| |
S149 |
14 | BAA10g10490 | A10 | 12235060 | C | T | downstream_gene_variant | MODIFIER | c.*2553C>T| |
S20 |
15 | BAA10g10490 | A10 | 12236208 | T | C | downstream_gene_variant | MODIFIER | c.*3701T>C| |
S223 |
16 | BAA10g10490 | A10 | 12236456 | C | T | downstream_gene_variant | MODIFIER | c.*3949C>T| |
S84 S93 |
17 | BAA10g10490 | A10 | 12237372 | C | T | downstream_gene_variant | MODIFIER | c.*4865C>T| |
S124 |