Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g16950 | A08 | 13877263 | C | T | upstream_gene_variant | MODIFIER | c.-4922C>T| |
S166 |
2 | BAA08g16950 | A08 | 13877293 | C | T | upstream_gene_variant | MODIFIER | c.-4892C>T| |
S111 |
3 | BAA08g16950 | A08 | 13877974 | G | A | upstream_gene_variant | MODIFIER | c.-4211G>A| |
S10 |
4 | BAA08g16950 | A08 | 13879035 | C | T | upstream_gene_variant | MODIFIER | c.-3150C>T| |
S247 |
5 | BAA08g16950 | A08 | 13879393 | G | A | upstream_gene_variant | MODIFIER | c.-2792G>A| |
S84 S93 |
6 | BAA08g16950 | A08 | 13881633 | C | T | upstream_gene_variant | MODIFIER | c.-552C>T| |
S83 S88 |
7 | BAA08g16950 | A08 | 13881823 | C | T | upstream_gene_variant | MODIFIER | c.-362C>T| |
S175 |
8 | BAA08g16950 | A08 | 13882501 | C | T | missense_variant | MODERATE | c.317C>T|p.Pro106Leu |
S216 |
9 | BAA08g16950 | A08 | 13882953 | C | T | missense_variant | MODERATE | c.769C>T|p.Leu257Phe |
S143 |
10 | BAA08g16950 | A08 | 13883933 | G | A | missense_variant | MODERATE | c.1749G>A|p.Met583Ile |
S260 |
11 | BAA08g16950 | A08 | 13884346 | C | T | missense_variant | MODERATE | c.2162C>T|p.Ser721Phe |
S53 |
12 | BAA08g16950 | A08 | 13884709 | G | A | missense_variant | MODERATE | c.2525G>A|p.Arg842Lys |
S183 |