Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g19190 | A08 | 15190968 | C | T | downstream_gene_variant | MODIFIER | c.*2805G>A| |
S223 |
2 | BAA08g19190 | A08 | 15191081 | C | T | downstream_gene_variant | MODIFIER | c.*2692G>A| |
S39 |
3 | BAA08g19190 | A08 | 15193925 | C | T | missense_variant | MODERATE | c.1327G>A|p.Ala443Thr |
S134 |
4 | BAA08g19190 | A08 | 15195958 | G | A | missense_variant | MODERATE | c.1048C>T|p.Leu350Phe |
S205 |
5 | BAA08g19190 | A08 | 15196019 | G | A | synonymous_variant | LOW | c.987C>T|p.Pro329Pro |
S246 |
6 | BAA08g19190 | A08 | 15196117 | G | A | missense_variant | MODERATE | c.889C>T|p.Pro297Ser |
S259 |
7 | BAA08g19190 | A08 | 15196482 | C | T | missense_variant&splice_region_variant | MODERATE | c.626G>A|p.Arg209Lys |
S86 |
8 | BAA08g19190 | A08 | 15197163 | G | A | missense_variant | MODERATE | c.43C>T|p.Leu15Phe |
S97 |
9 | BAA08g19190 | A08 | 15198051 | C | T | upstream_gene_variant | MODIFIER | c.-846G>A| |
S171 |
10 | BAA08g19190 | A08 | 15199017 | C | T | upstream_gene_variant | MODIFIER | c.-1812G>A| |
S61 |
11 | BAA08g19190 | A08 | 15199636 | C | T | upstream_gene_variant | MODIFIER | c.-2431G>A| |
S213 |
12 | BAA08g19190 | A08 | 15199682 | G | A | upstream_gene_variant | MODIFIER | c.-2477C>T| |
S62 |
13 | BAA08g19190 | A08 | 15199928 | G | A | upstream_gene_variant | MODIFIER | c.-2723C>T| |
S179 |
14 | BAA08g19190 | A08 | 15200664 | G | A | upstream_gene_variant | MODIFIER | c.-3459C>T| |
S98 |
15 | BAA08g19190 | A08 | 15201960 | G | A | upstream_gene_variant | MODIFIER | c.-4755C>T| |
S146 |