Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26540 | A02 | 14824415 | G | A | synonymous_variant | LOW | c.1726C>T|p.Leu576Leu |
S103 |
2 | BAA02g26540 | A02 | 14824452 | C | T | stop_gained&splice_region_variant | HIGH | c.1689G>A|p.Trp563* |
S164 |
3 | BAA02g26540 | A02 | 14825492 | G | A | missense_variant | MODERATE | c.1060C>T|p.Pro354Ser |
S249 |
4 | BAA02g26540 | A02 | 14825546 | G | A | missense_variant | MODERATE | c.1006C>T|p.Leu336Phe |
S271 |
5 | BAA02g26540 | A02 | 14825822 | G | A | missense_variant | MODERATE | c.802C>T|p.His268Tyr |
S288 |
6 | BAA02g26540 | A02 | 14826049 | G | A | synonymous_variant | LOW | c.657C>T|p.Phe219Phe |
S247 |
7 | BAA02g26540 | A02 | 14826114 | C | T | missense_variant | MODERATE | c.592G>A|p.Glu198Lys |
S112 |
8 | BAA02g26540 | A02 | 14827139 | C | T | upstream_gene_variant | MODIFIER | c.-434G>A| |
S287 |
9 | BAA02g26540 | A02 | 14827221 | G | A | upstream_gene_variant | MODIFIER | c.-516C>T| |
S173 S176 |
10 | BAA02g26540 | A02 | 14829189 | G | A | upstream_gene_variant | MODIFIER | c.-2484C>T| |
S169 |
11 | BAA02g26540 | A02 | 14830116 | G | A | upstream_gene_variant | MODIFIER | c.-3411C>T| |
S134 |
12 | BAA02g26540 | A02 | 14830555 | G | A | upstream_gene_variant | MODIFIER | c.-3850C>T| |
S55 |
13 | BAA02g26540 | A02 | 14831277 | G | A | upstream_gene_variant | MODIFIER | c.-4572C>T| |
S68 |
14 | BAA02g26540 | A02 | 14831445 | G | A | upstream_gene_variant | MODIFIER | c.-4740C>T| |
S5 |
15 | BAA02g26540 | A02 | 14831637 | G | A | upstream_gene_variant | MODIFIER | c.-4932C>T| |
S169 |