Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g16450 | A01 | 7991470 | C | T | missense_variant | MODERATE | c.944G>A|p.Gly315Asp |
S136 |
2 | BAA01g16450 | A01 | 7991473 | C | T | missense_variant | MODERATE | c.941G>A|p.Gly314Glu |
S166 |
3 | BAA01g16450 | A01 | 7992059 | G | A | missense_variant | MODERATE | c.533C>T|p.Thr178Met |
S268 |
4 | BAA01g16450 | A01 | 7992127 | G | A | synonymous_variant | LOW | c.465C>T|p.His155His |
S256 |
5 | BAA01g16450 | A01 | 7992601 | G | A | missense_variant | MODERATE | c.239C>T|p.Ser80Phe |
S13 |
6 | BAA01g16450 | A01 | 7992929 | G | A | missense_variant | MODERATE | c.88C>T|p.Leu30Phe |
S57 |
7 | BAA01g16450 | A01 | 7992990 | G | A | synonymous_variant | LOW | c.27C>T|p.His9His |
S108 |
8 | BAA01g16450 | A01 | 7996371 | G | A | upstream_gene_variant | MODIFIER | c.-3355C>T| |
S131 |
9 | BAA01g16450 | A01 | 7996479 | C | T | upstream_gene_variant | MODIFIER | c.-3463G>A| |
S265 |
10 | BAA01g16450 | A01 | 7996906 | G | A | upstream_gene_variant | MODIFIER | c.-3890C>T| |
S251 |
11 | BAA01g16450 | A01 | 7997376 | G | A | upstream_gene_variant | MODIFIER | c.-4360C>T| |
S180 |