Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g59160 | A03 | 29611715 | C | T | upstream_gene_variant | MODIFIER | c.-4567C>T| |
S113 |
2 | BAA03g59160 | A03 | 29612012 | C | T | upstream_gene_variant | MODIFIER | c.-4270C>T| |
S281 |
3 | BAA03g59160 | A03 | 29612467 | C | T | upstream_gene_variant | MODIFIER | c.-3815C>T| |
S40 S49 |
4 | BAA03g59160 | A03 | 29612589 | C | T | upstream_gene_variant | MODIFIER | c.-3693C>T| |
S293 |
5 | BAA03g59160 | A03 | 29616469 | C | T | missense_variant | MODERATE | c.188C>T|p.Pro63Leu |
S281 |
6 | BAA03g59160 | A03 | 29617012 | C | T | missense_variant | MODERATE | c.731C>T|p.Pro244Leu |
S216 S241 S39 |
7 | BAA03g59160 | A03 | 29617795 | G | A | missense_variant | MODERATE | c.1514G>A|p.Gly505Glu |
S13 S140 S279 S64 |
8 | BAA03g59160 | A03 | 29617851 | C | T | missense_variant | MODERATE | c.1570C>T|p.Pro524Ser |
S8 |
9 | BAA03g59160 | A03 | 29617873 | C | T | missense_variant | MODERATE | c.1592C>T|p.Ser531Phe |
S89 |
10 | BAA03g59160 | A03 | 29618781 | C | T | missense_variant | MODERATE | c.2500C>T|p.His834Tyr |
S3 |
11 | BAA03g59160 | A03 | 29619077 | G | A | synonymous_variant | LOW | c.2796G>A|p.Lys932Lys |
S242 |
12 | BAA03g59160 | A03 | 29619739 | C | T | downstream_gene_variant | MODIFIER | c.*161C>T| |
S292 |