Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00450 | A10 | 205963 | C | T | downstream_gene_variant | MODIFIER | c.*4071G>A| |
S286 |
2 | BAA10g00450 | A10 | 211562 | C | T | missense_variant | MODERATE | c.856G>A|p.Glu286Lys |
S129 |
3 | BAA10g00450 | A10 | 211824 | G | A | synonymous_variant | LOW | c.594C>T|p.Phe198Phe |
S65 |
4 | BAA10g00450 | A10 | 211876 | G | A | missense_variant | MODERATE | c.542C>T|p.Ser181Phe |
S280 |
5 | BAA10g00450 | A10 | 211933 | G | A | missense_variant | MODERATE | c.485C>T|p.Ala162Val |
S18 |
6 | BAA10g00450 | A10 | 212099 | C | T | missense_variant | MODERATE | c.319G>A|p.Asp107Asn |
S159 S243 S298 S299 |
7 | BAA10g00450 | A10 | 212193 | G | A | synonymous_variant | LOW | c.225C>T|p.Ser75Ser |
S164 |
8 | BAA10g00450 | A10 | 212359 | G | A | missense_variant | MODERATE | c.59C>T|p.Ser20Leu |
S293 |
9 | BAA10g00450 | A10 | 213224 | G | A | upstream_gene_variant | MODIFIER | c.-807C>T| |
S39 |
10 | BAA10g00450 | A10 | 216290 | G | A | upstream_gene_variant | MODIFIER | c.-3873C>T| |
S284 |