Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00290 | A08 | 214122 | C | T | downstream_gene_variant | MODIFIER | c.*972G>A| |
S245 |
2 | BAA08g00290 | A08 | 214600 | G | A | downstream_gene_variant | MODIFIER | c.*494C>T| |
S158 |
3 | BAA08g00290 | A08 | 214627 | C | T | downstream_gene_variant | MODIFIER | c.*467G>A| |
S209 |
4 | BAA08g00290 | A08 | 215347 | G | A | missense_variant | MODERATE | c.1646C>T|p.Pro549Leu |
S40 S49 |
5 | BAA08g00290 | A08 | 215809 | C | T | splice_donor_variant&intron_variant | HIGH | c.1302+1G>A| |
S173 |
6 | BAA08g00290 | A08 | 216224 | C | T | missense_variant | MODERATE | c.976G>A|p.Ala326Thr |
S149 |
7 | BAA08g00290 | A08 | 216286 | C | T | missense_variant | MODERATE | c.914G>A|p.Gly305Glu |
S76 |
8 | BAA08g00290 | A08 | 216496 | C | T | missense_variant | MODERATE | c.775G>A|p.Val259Ile |
S291 |
9 | BAA08g00290 | A08 | 216845 | C | T | missense_variant | MODERATE | c.502G>A|p.Ala168Thr |
S233 |
10 | BAA08g00290 | A08 | 217215 | C | T | stop_gained | HIGH | c.132G>A|p.Trp44* |
S106 |
11 | BAA08g00290 | A08 | 217281 | C | T | synonymous_variant | LOW | c.66G>A|p.Gly22Gly |
S28 |
12 | BAA08g00290 | A08 | 217392 | G | A | upstream_gene_variant | MODIFIER | c.-46C>T| |
S260 |
13 | BAA08g00290 | A08 | 217530 | C | T | upstream_gene_variant | MODIFIER | c.-184G>A| |
S303 |
14 | BAA08g00290 | A08 | 220761 | C | T | upstream_gene_variant | MODIFIER | c.-3415G>A| |
S203 |
15 | BAA08g00290 | A08 | 221457 | C | T | upstream_gene_variant | MODIFIER | c.-4111G>A| |
S201 |
16 | BAA08g00290 | A08 | 222020 | G | A | upstream_gene_variant | MODIFIER | c.-4674C>T| |
S200 |
17 | BAA08g00290 | A08 | 222032 | C | T | upstream_gene_variant | MODIFIER | c.-4686G>A| |
S142 |