Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18190 | A10 | 17132630 | C | T | missense_variant | MODERATE | c.929G>A|p.Cys310Tyr |
S2 |
2 | BAA10g18190 | A10 | 17133066 | C | T | missense_variant | MODERATE | c.493G>A|p.Glu165Lys |
S281 |
3 | BAA10g18190 | A10 | 17133110 | G | A | missense_variant | MODERATE | c.449C>T|p.Ala150Val |
S65 |
4 | BAA10g18190 | A10 | 17133348 | G | A | missense_variant | MODERATE | c.211C>T|p.Pro71Ser |
S132 S215 S89 |
5 | BAA10g18190 | A10 | 17133364 | G | A | synonymous_variant | LOW | c.195C>T|p.Thr65Thr |
S128 |
6 | BAA10g18190 | A10 | 17133485 | G | A | missense_variant | MODERATE | c.74C>T|p.Pro25Leu |
S113 |
7 | BAA10g18190 | A10 | 17133521 | G | A | missense_variant | MODERATE | c.38C>T|p.Ser13Phe |
S72 S78 |
8 | BAA10g18190 | A10 | 17137595 | G | A | upstream_gene_variant | MODIFIER | c.-4037C>T| |
S100 |
9 | BAA10g18190 | A10 | 17138304 | C | T | upstream_gene_variant | MODIFIER | c.-4746G>A| |
S130 |