Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g34130 | A06 | 22952218 | T | A | missense_variant | MODERATE | c.976A>T|p.Thr326Ser |
S119 |
2 | BAA06g34130 | A06 | 22953013 | G | A | synonymous_variant | LOW | c.654C>T|p.Ile218Ile |
S153 S157 S166 S167 S257 S263 |
3 | BAA06g34130 | A06 | 22954692 | C | T | upstream_gene_variant | MODIFIER | c.-670G>A| |
S296 |
4 | BAA06g34130 | A06 | 22954715 | C | T | upstream_gene_variant | MODIFIER | c.-693G>A| |
S295 |
5 | BAA06g34130 | A06 | 22955854 | C | T | upstream_gene_variant | MODIFIER | c.-1832G>A| |
S70 |
6 | BAA06g34130 | A06 | 22956260 | C | T | upstream_gene_variant | MODIFIER | c.-2238G>A| |
S186 |
7 | BAA06g34130 | A06 | 22956924 | C | T | upstream_gene_variant | MODIFIER | c.-2902G>A| |
S111 |
8 | BAA06g34130 | A06 | 22957572 | C | A | upstream_gene_variant | MODIFIER | c.-3550G>T| |
S20 |
9 | BAA06g34130 | A06 | 22957813 | G | A | upstream_gene_variant | MODIFIER | c.-3791C>T| |
S131 |
10 | BAA06g34130 | A06 | 22958003 | C | T | upstream_gene_variant | MODIFIER | c.-3981G>A| |
S79 S91 |
11 | BAA06g34130 | A06 | 22958021 | G | A | upstream_gene_variant | MODIFIER | c.-3999C>T| |
S140 |
12 | BAA06g34130 | A06 | 22958219 | G | A | upstream_gene_variant | MODIFIER | c.-4197C>T| |
S41 |
13 | BAA06g34130 | A06 | 22958736 | G | A | upstream_gene_variant | MODIFIER | c.-4714C>T| |
S12 |
14 | BAA06g34130 | A06 | 22958823 | C | T | upstream_gene_variant | MODIFIER | c.-4801G>A| |
S267 |
15 | BAA06g34130 | A06 | 22958991 | G | A | upstream_gene_variant | MODIFIER | c.-4969C>T| |
S50 |