Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01440 | A10 | 730025 | C | T | upstream_gene_variant | MODIFIER | c.-114C>T| |
S144 |
2 | BAA10g01440 | A10 | 730406 | G | A | missense_variant | MODERATE | c.268G>A|p.Glu90Lys |
S274 |
3 | BAA10g01440 | A10 | 730440 | G | A | missense_variant | MODERATE | c.302G>A|p.Gly101Asp |
S217 S248 |
4 | BAA10g01440 | A10 | 731319 | C | T | missense_variant | MODERATE | c.455C>T|p.Thr152Ile |
S175 |
5 | BAA10g01440 | A10 | 731387 | G | A | missense_variant | MODERATE | c.523G>A|p.Glu175Lys |
S303 |
6 | BAA10g01440 | A10 | 732260 | C | T | missense_variant | MODERATE | c.1106C>T|p.Pro369Leu |
S60 |
7 | BAA10g01440 | A10 | 732555 | G | A | synonymous_variant | LOW | c.1401G>A|p.Arg467Arg |
S228 |
8 | BAA10g01440 | A10 | 732568 | G | A | missense_variant | MODERATE | c.1414G>A|p.Ala472Thr |
S151 S263 |
9 | BAA10g01440 | A10 | 732586 | G | A | missense_variant | MODERATE | c.1432G>A|p.Gly478Arg |
S76 |
10 | BAA10g01440 | A10 | 733372 | C | T | missense_variant | MODERATE | c.2218C>T|p.Pro740Ser |
S294 |