Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06540 | A10 | 3399286 | C | T | missense_variant | MODERATE | c.886G>A|p.Gly296Arg |
S242 |
2 | BAA10g06540 | A10 | 3399394 | C | T | missense_variant | MODERATE | c.778G>A|p.Asp260Asn |
S233 |
3 | BAA10g06540 | A10 | 3399456 | C | T | missense_variant | MODERATE | c.716G>A|p.Gly239Glu |
S11 |
4 | BAA10g06540 | A10 | 3399557 | G | A | synonymous_variant | LOW | c.615C>T|p.Asp205Asp |
S97 |
5 | BAA10g06540 | A10 | 3400270 | G | A | missense_variant | MODERATE | c.116C>T|p.Ser39Phe |
S274 |
6 | BAA10g06540 | A10 | 3400408 | G | A | upstream_gene_variant | MODIFIER | c.-23C>T| |
S292 |
7 | BAA10g06540 | A10 | 3403829 | C | T | upstream_gene_variant | MODIFIER | c.-3444G>A| |
S131 |
8 | BAA10g06540 | A10 | 3403876 | C | T | upstream_gene_variant | MODIFIER | c.-3491G>A| |
S159 S243 S299 |
9 | BAA10g06540 | A10 | 3403998 | T | A | upstream_gene_variant | MODIFIER | c.-3613A>T| |
S26 |