Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09220 | A02 | 4075760 | G | A | synonymous_variant | LOW | c.1146C>T|p.Arg382Arg |
S177 |
2 | BAA02g09220 | A02 | 4075817 | G | A | synonymous_variant | LOW | c.1089C>T|p.Ile363Ile |
S282 |
3 | BAA02g09220 | A02 | 4076022 | G | A | missense_variant | MODERATE | c.884C>T|p.Ala295Val |
S45 |
4 | BAA02g09220 | A02 | 4076049 | G | A | missense_variant | MODERATE | c.857C>T|p.Ala286Val |
S134 |
5 | BAA02g09220 | A02 | 4076116 | G | A | missense_variant | MODERATE | c.790C>T|p.Leu264Phe |
S275 |
6 | BAA02g09220 | A02 | 4077280 | C | T | intron_variant | MODIFIER | c.582-887G>A| |
S262 |
7 | BAA02g09220 | A02 | 4082673 | C | T | missense_variant | MODERATE | c.49G>A|p.Asp17Asn |
S46 |
8 | BAA02g09220 | A02 | 4085469 | C | T | upstream_gene_variant | MODIFIER | c.-2748G>A| |
S94 |
9 | BAA02g09220 | A02 | 4086288 | C | T | upstream_gene_variant | MODIFIER | c.-3567G>A| |
S127 |
10 | BAA02g09220 | A02 | 4086552 | C | T | upstream_gene_variant | MODIFIER | c.-3831G>A| |
S278 |
11 | BAA02g09220 | A02 | 4086975 | C | T | upstream_gene_variant | MODIFIER | c.-4254G>A| |
S283 |
12 | BAA02g09220 | A02 | 4086981 | G | A | upstream_gene_variant | MODIFIER | c.-4260C>T| |
S132 S137 S215 |
13 | BAA02g09220 | A02 | 4087011 | C | T | upstream_gene_variant | MODIFIER | c.-4290G>A| |
S54 |
14 | BAA02g09220 | A02 | 4087199 | G | A | upstream_gene_variant | MODIFIER | c.-4478C>T| |
S114 |