Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g22800 | A03 | 10387502 | G | A | synonymous_variant | LOW | c.1203C>T|p.Ala401Ala |
S169 |
2 | BAA03g22800 | A03 | 10387535 | G | A | synonymous_variant | LOW | c.1170C>T|p.His390His |
S246 |
3 | BAA03g22800 | A03 | 10387691 | G | A | synonymous_variant | LOW | c.1014C>T|p.Val338Val |
S198 |
4 | BAA03g22800 | A03 | 10388256 | C | T | missense_variant | MODERATE | c.766G>A|p.Glu256Lys |
S236 |
5 | BAA03g22800 | A03 | 10388358 | C | T | missense_variant | MODERATE | c.664G>A|p.Ala222Thr |
S274 |
6 | BAA03g22800 | A03 | 10389193 | C | T | missense_variant | MODERATE | c.301G>A|p.Glu101Lys |
S155 |
7 | BAA03g22800 | A03 | 10389467 | C | T | synonymous_variant | LOW | c.27G>A|p.Ala9Ala |
S190 |
8 | BAA03g22800 | A03 | 10391051 | C | T | upstream_gene_variant | MODIFIER | c.-1558G>A| |
S91 |
9 | BAA03g22800 | A03 | 10391446 | C | T | upstream_gene_variant | MODIFIER | c.-1953G>A| |
S112 |
10 | BAA03g22800 | A03 | 10393415 | C | T | upstream_gene_variant | MODIFIER | c.-3922G>A| |
S216 |
11 | BAA03g22800 | A03 | 10393761 | G | A | upstream_gene_variant | MODIFIER | c.-4268C>T| |
S10 |
12 | BAA03g22800 | A03 | 10394018 | C | T | upstream_gene_variant | MODIFIER | c.-4525G>A| |
S250 |