Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g66280 | A03 | 40605654 | G | A | splice_region_variant&intron_variant | LOW | c.1107+7C>T| |
S127 |
2 | BAA03g66280 | A03 | 40605672 | C | T | missense_variant | MODERATE | c.1096G>A|p.Asp366Asn |
S174 |
3 | BAA03g66280 | A03 | 40605925 | G | A | synonymous_variant | LOW | c.928C>T|p.Leu310Leu |
S276 |
4 | BAA03g66280 | A03 | 40606609 | G | A | synonymous_variant | LOW | c.621C>T|p.Ser207Ser |
S271 |
5 | BAA03g66280 | A03 | 40606894 | G | A | missense_variant | MODERATE | c.437C>T|p.Ser146Phe |
S294 |
6 | BAA03g66280 | A03 | 40609273 | C | T | upstream_gene_variant | MODIFIER | c.-1732G>A| |
S298 |
7 | BAA03g66280 | A03 | 40611506 | G | A | upstream_gene_variant | MODIFIER | c.-3965C>T| |
S282 |
8 | BAA03g66280 | A03 | 40611643 | C | T | upstream_gene_variant | MODIFIER | c.-4102G>A| |
S279 |
9 | BAA03g66280 | A03 | 40611734 | C | T | upstream_gene_variant | MODIFIER | c.-4193G>A| |
S252 |
10 | BAA03g66280 | A03 | 40612392 | G | A | upstream_gene_variant | MODIFIER | c.-4851C>T| |
S128 |