Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g19980 | A08 | 15569187 | C | T | upstream_gene_variant | MODIFIER | c.-4132C>T| |
S217 |
2 | BAA08g19980 | A08 | 15569507 | C | T | upstream_gene_variant | MODIFIER | c.-3812C>T| |
S80 |
3 | BAA08g19980 | A08 | 15570406 | C | T | upstream_gene_variant | MODIFIER | c.-2913C>T| |
S139 |
4 | BAA08g19980 | A08 | 15571737 | C | T | upstream_gene_variant | MODIFIER | c.-1582C>T| |
S92 |
5 | BAA08g19980 | A08 | 15572345 | C | T | upstream_gene_variant | MODIFIER | c.-974C>T| |
S110 |
6 | BAA08g19980 | A08 | 15572861 | G | A | upstream_gene_variant | MODIFIER | c.-458G>A| |
S159 S187 S188 S243 S276 S298 |
7 | BAA08g19980 | A08 | 15573410 | G | A | missense_variant | MODERATE | c.92G>A|p.Gly31Glu |
S68 |
8 | BAA08g19980 | A08 | 15573476 | C | T | missense_variant | MODERATE | c.158C>T|p.Ser53Phe |
S161 |
9 | BAA08g19980 | A08 | 15574581 | G | A | missense_variant | MODERATE | c.260G>A|p.Gly87Asp |
S225 S73 |
10 | BAA08g19980 | A08 | 15574607 | C | T | missense_variant | MODERATE | c.286C>T|p.His96Tyr |
S215 |
11 | BAA08g19980 | A08 | 15574709 | G | A | splice_donor_variant&intron_variant | HIGH | c.387+1G>A| |
S42 |
12 | BAA08g19980 | A08 | 15575882 | G | A | missense_variant&splice_region_variant | MODERATE | c.1160G>A|p.Arg387Lys |
S289 S290 |
13 | BAA08g19980 | A08 | 15576342 | G | A | missense_variant | MODERATE | c.1438G>A|p.Gly480Arg |
S238 |