Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g25160 | A06 | 17057984 | C | T | synonymous_variant | LOW | c.234C>T|p.Phe78Phe |
S302 |
2 | BAA06g25160 | A06 | 17058436 | C | T | missense_variant | MODERATE | c.527C>T|p.Ser176Phe |
S236 |
3 | BAA06g25160 | A06 | 17059300 | G | A | missense_variant | MODERATE | c.1391G>A|p.Gly464Asp |
S130 |
4 | BAA06g25160 | A06 | 17059549 | C | T | missense_variant | MODERATE | c.1640C>T|p.Ala547Val |
S95 |
5 | BAA06g25160 | A06 | 17059854 | G | A | missense_variant | MODERATE | c.1945G>A|p.Asp649Asn |
S8 |
6 | BAA06g25160 | A06 | 17059991 | C | T | synonymous_variant | LOW | c.2082C>T|p.Thr694Thr |
S42 |
7 | BAA06g25160 | A06 | 17060382 | G | A | missense_variant | MODERATE | c.2473G>A|p.Val825Met |
S190 |
8 | BAA06g25160 | A06 | 17060727 | G | A | synonymous_variant | LOW | c.2754G>A|p.Gln918Gln |
S20 |
9 | BAA06g25160 | A06 | 17060776 | C | T | synonymous_variant | LOW | c.2803C>T|p.Leu935Leu |
S298 |
10 | BAA06g25160 | A06 | 17061514 | C | T | downstream_gene_variant | MODIFIER | c.*583C>T| |
S192 |
11 | BAA06g25160 | A06 | 17061845 | C | T | downstream_gene_variant | MODIFIER | c.*914C>T| |
S296 |
12 | BAA06g25160 | A06 | 17062106 | G | A | downstream_gene_variant | MODIFIER | c.*1175G>A| |
S180 |