Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g67650 | A09 | 61193427 | C | T | missense_variant | MODERATE | c.3085G>A|p.Gly1029Arg |
S192 |
2 | BAA09g67650 | A09 | 61194795 | G | A | missense_variant | MODERATE | c.2279C>T|p.Ser760Leu |
S15 S3 |
3 | BAA09g67650 | A09 | 61196439 | C | T | missense_variant | MODERATE | c.1364G>A|p.Gly455Glu |
S272 |
4 | BAA09g67650 | A09 | 61196699 | G | A | synonymous_variant | LOW | c.1104C>T|p.Leu368Leu |
S25 |
5 | BAA09g67650 | A09 | 61196721 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1083-1G>A| |
S185 |
6 | BAA09g67650 | A09 | 61197258 | C | T | missense_variant | MODERATE | c.973G>A|p.Val325Ile |
S267 |
7 | BAA09g67650 | A09 | 61198046 | C | T | missense_variant | MODERATE | c.257G>A|p.Cys86Tyr |
S172 S217 |
8 | BAA09g67650 | A09 | 61198471 | C | T | upstream_gene_variant | MODIFIER | c.-169G>A| |
S136 |
9 | BAA09g67650 | A09 | 61201285 | C | T | upstream_gene_variant | MODIFIER | c.-2983G>A| |
S94 |
10 | BAA09g67650 | A09 | 61201670 | C | T | upstream_gene_variant | MODIFIER | c.-3368G>A| |
S135 S203 |