Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g19610 | A06 | 10156256 | G | A | upstream_gene_variant | MODIFIER | c.-2738G>A| |
S208 S219 |
2 | BAA06g19610 | A06 | 10159075 | C | T | missense_variant | MODERATE | c.82C>T|p.Pro28Ser |
S96 |
3 | BAA06g19610 | A06 | 10159408 | C | T | missense_variant | MODERATE | c.415C>T|p.Leu139Phe |
S159 S243 S299 |
4 | BAA06g19610 | A06 | 10159528 | G | A | missense_variant | MODERATE | c.535G>A|p.Glu179Lys |
S197 |
5 | BAA06g19610 | A06 | 10159889 | G | A | missense_variant | MODERATE | c.731G>A|p.Gly244Glu |
S295 |
6 | BAA06g19610 | A06 | 10160435 | G | A | synonymous_variant | LOW | c.1062G>A|p.Lys354Lys |
S272 |
7 | BAA06g19610 | A06 | 10161141 | C | T | splice_region_variant&intron_variant | LOW | c.1501-5C>T| |
S135 |
8 | BAA06g19610 | A06 | 10161981 | G | A | synonymous_variant | LOW | c.2259G>A|p.Leu753Leu |
S213 |
9 | BAA06g19610 | A06 | 10162102 | G | A | missense_variant | MODERATE | c.2380G>A|p.Glu794Lys |
S1 S90 |
10 | BAA06g19610 | A06 | 10162586 | C | T | downstream_gene_variant | MODIFIER | c.*71C>T| |
S172 S217 |
11 | BAA06g19610 | A06 | 10164488 | G | A | downstream_gene_variant | MODIFIER | c.*1973G>A| |
S224 |