Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g07580 | A01 | 3342136 | G | A | upstream_gene_variant | MODIFIER | c.-1378G>A| |
S289 S290 |
2 | BAA01g07580 | A01 | 3342617 | C | T | upstream_gene_variant | MODIFIER | c.-897C>T| |
S291 |
3 | BAA01g07580 | A01 | 3342723 | G | T | upstream_gene_variant | MODIFIER | c.-791G>T| |
S14 |
4 | BAA01g07580 | A01 | 3342935 | G | A | upstream_gene_variant | MODIFIER | c.-579G>A| |
S122 |
5 | BAA01g07580 | A01 | 3343692 | C | T | missense_variant | MODERATE | c.179C>T|p.Ser60Phe |
S132 S137 S215 |
6 | BAA01g07580 | A01 | 3344189 | C | T | missense_variant | MODERATE | c.676C>T|p.Leu226Phe |
S81 S85 |
7 | BAA01g07580 | A01 | 3344834 | G | A | missense_variant | MODERATE | c.1321G>A|p.Ala441Thr |
S15 |
8 | BAA01g07580 | A01 | 3344942 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1360-1G>A| |
S262 |
9 | BAA01g07580 | A01 | 3345032 | G | A | synonymous_variant | LOW | c.1449G>A|p.Glu483Glu |
S181 |
10 | BAA01g07580 | A01 | 3345152 | G | A | synonymous_variant | LOW | c.1485G>A|p.Val495Val |
S146 |