Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g26930 | A08 | 19090903 | G | A | missense_variant | MODERATE | c.2380C>T|p.Pro794Ser |
S256 |
2 | BAA08g26930 | A08 | 19090999 | C | T | missense_variant | MODERATE | c.2284G>A|p.Val762Ile |
S88 |
3 | BAA08g26930 | A08 | 19091011 | G | A | missense_variant | MODERATE | c.2272C>T|p.Pro758Ser |
S157 |
4 | BAA08g26930 | A08 | 19091145 | G | A | missense_variant | MODERATE | c.2138C>T|p.Ser713Phe |
S205 |
5 | BAA08g26930 | A08 | 19091242 | G | A | missense_variant | MODERATE | c.2041C>T|p.Pro681Ser |
S279 |
6 | BAA08g26930 | A08 | 19091667 | G | A | missense_variant | MODERATE | c.1616C>T|p.Ser539Phe |
S100 |
7 | BAA08g26930 | A08 | 19092175 | G | A | missense_variant | MODERATE | c.1108C>T|p.His370Tyr |
S190 |
8 | BAA08g26930 | A08 | 19092235 | G | A | missense_variant | MODERATE | c.1048C>T|p.Pro350Ser |
S161 S282 |
9 | BAA08g26930 | A08 | 19092258 | G | A | missense_variant | MODERATE | c.1025C>T|p.Ser342Phe |
S176 |
10 | BAA08g26930 | A08 | 19093452 | C | T | upstream_gene_variant | MODIFIER | c.-170G>A| |
S191 S236 |
11 | BAA08g26930 | A08 | 19094194 | C | T | upstream_gene_variant | MODIFIER | c.-912G>A| |
S189 |
12 | BAA08g26930 | A08 | 19096621 | G | A | upstream_gene_variant | MODIFIER | c.-3339C>T| |
S176 |
13 | BAA08g26930 | A08 | 19097228 | C | T | upstream_gene_variant | MODIFIER | c.-3946G>A| |
S59 |
14 | BAA08g26930 | A08 | 19097836 | C | T | upstream_gene_variant | MODIFIER | c.-4554G>A| |
S105 S106 |