Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44340 | A09 | 50063472 | G | A | missense_variant | MODERATE | c.2981C>T|p.Pro994Leu |
S156 |
2 | BAA09g44340 | A09 | 50063644 | C | T | missense_variant | MODERATE | c.2809G>A|p.Val937Ile |
S6 |
3 | BAA09g44340 | A09 | 50065661 | C | T | synonymous_variant | LOW | c.1074G>A|p.Lys358Lys |
S182 |
4 | BAA09g44340 | A09 | 50065842 | G | A | missense_variant | MODERATE | c.893C>T|p.Ser298Phe |
S264 |
5 | BAA09g44340 | A09 | 50066233 | G | A | synonymous_variant | LOW | c.502C>T|p.Leu168Leu |
S194 |
6 | BAA09g44340 | A09 | 50067545 | C | T | missense_variant | MODERATE | c.332G>A|p.Ser111Asn |
S103 |
7 | BAA09g44340 | A09 | 50067737 | G | A | missense_variant | MODERATE | c.140C>T|p.Ser47Phe |
S193 |
8 | BAA09g44340 | A09 | 50067918 | C | T | upstream_gene_variant | MODIFIER | c.-42G>A| |
S146 |
9 | BAA09g44340 | A09 | 50068222 | G | A | upstream_gene_variant | MODIFIER | c.-346C>T| |
S16 |
10 | BAA09g44340 | A09 | 50071538 | C | T | upstream_gene_variant | MODIFIER | c.-3662G>A| |
S260 |
11 | BAA09g44340 | A09 | 50072669 | G | A | upstream_gene_variant | MODIFIER | c.-4793C>T| |
S4 |