Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g49070 | A09 | 52615771 | C | T | missense_variant | MODERATE | c.2687G>A|p.Gly896Glu |
S65 |
2 | BAA09g49070 | A09 | 52617005 | C | T | missense_variant | MODERATE | c.1453G>A|p.Glu485Lys |
S152 |
3 | BAA09g49070 | A09 | 52617674 | C | T | synonymous_variant | LOW | c.1197G>A|p.Leu399Leu |
S115 |
4 | BAA09g49070 | A09 | 52618434 | C | T | missense_variant | MODERATE | c.437G>A|p.Cys146Tyr |
S245 |
5 | BAA09g49070 | A09 | 52618536 | G | A | missense_variant | MODERATE | c.335C>T|p.Thr112Ile |
S2 |
6 | BAA09g49070 | A09 | 52618589 | G | A | synonymous_variant | LOW | c.282C>T|p.Leu94Leu |
S190 |
7 | BAA09g49070 | A09 | 52618747 | C | T | missense_variant | MODERATE | c.124G>A|p.Asp42Asn |
S120 |
8 | BAA09g49070 | A09 | 52619273 | G | A | upstream_gene_variant | MODIFIER | c.-403C>T| |
S67 |
9 | BAA09g49070 | A09 | 52619856 | C | T | upstream_gene_variant | MODIFIER | c.-986G>A| |
S68 |
10 | BAA09g49070 | A09 | 52619886 | G | A | upstream_gene_variant | MODIFIER | c.-1016C>T| |
S192 |
11 | BAA09g49070 | A09 | 52620164 | C | T | upstream_gene_variant | MODIFIER | c.-1294G>A| |
S301 S304 |
12 | BAA09g49070 | A09 | 52620239 | G | A | upstream_gene_variant | MODIFIER | c.-1369C>T| |
S177 |