Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18260 | A10 | 17156144 | C | T | stop_gained&splice_region_variant | HIGH | c.670C>T|p.Gln224* |
S18 |
2 | BAA10g18260 | A10 | 17156708 | G | A | synonymous_variant | LOW | c.912G>A|p.Lys304Lys |
S208 S219 |
3 | BAA10g18260 | A10 | 17157136 | G | A | missense_variant | MODERATE | c.973G>A|p.Glu325Lys |
S278 |
4 | BAA10g18260 | A10 | 17157253 | C | T | missense_variant&splice_region_variant | MODERATE | c.1090C>T|p.Pro364Ser |
S204 |
5 | BAA10g18260 | A10 | 17158471 | G | A | missense_variant | MODERATE | c.2021G>A|p.Gly674Glu |
S273 |
6 | BAA10g18260 | A10 | 17158547 | C | T | synonymous_variant | LOW | c.2097C>T|p.Asn699Asn |
S10 |
7 | BAA10g18260 | A10 | 17158629 | C | T | synonymous_variant | LOW | c.2179C>T|p.Leu727Leu |
S200 |
8 | BAA10g18260 | A10 | 17159352 | C | T | missense_variant | MODERATE | c.2545C>T|p.His849Tyr |
S238 |