Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00070 | A10 | 20802 | C | T | missense_variant | MODERATE | c.1288G>A|p.Ala430Thr |
S68 |
2 | BAA10g00070 | A10 | 21714 | G | A | missense_variant | MODERATE | c.887C>T|p.Ala296Val |
S156 |
3 | BAA10g00070 | A10 | 22934 | G | A | synonymous_variant | LOW | c.537C>T|p.Ser179Ser |
S45 |
4 | BAA10g00070 | A10 | 23018 | G | A | splice_region_variant&synonymous_variant | LOW | c.453C>T|p.Tyr151Tyr |
S289 |
5 | BAA10g00070 | A10 | 24333 | C | T | upstream_gene_variant | MODIFIER | c.-497G>A| |
S23 |
6 | BAA10g00070 | A10 | 25440 | G | A | upstream_gene_variant | MODIFIER | c.-1604C>T| |
S48 |
7 | BAA10g00070 | A10 | 28161 | C | T | upstream_gene_variant | MODIFIER | c.-4325G>A| |
S271 |