Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11870 | A01 | 5553591 | C | T | synonymous_variant | LOW | c.4866G>A|p.Val1622Val |
S18 |
2 | BAA01g11870 | A01 | 5553729 | G | A | synonymous_variant | LOW | c.4728C>T|p.Arg1576Arg |
S138 |
3 | BAA01g11870 | A01 | 5553990 | G | A | synonymous_variant | LOW | c.4467C>T|p.Arg1489Arg |
S165 |
4 | BAA01g11870 | A01 | 5554272 | G | A | synonymous_variant | LOW | c.4185C>T|p.Leu1395Leu |
S201 |
5 | BAA01g11870 | A01 | 5554613 | C | T | missense_variant | MODERATE | c.3844G>A|p.Ala1282Thr |
S167 |
6 | BAA01g11870 | A01 | 5554932 | C | T | missense_variant | MODERATE | c.3525G>A|p.Met1175Ile |
S18 |
7 | BAA01g11870 | A01 | 5555125 | C | T | missense_variant | MODERATE | c.3332G>A|p.Ser1111Asn |
S225 S73 |
8 | BAA01g11870 | A01 | 5555439 | G | A | missense_variant | MODERATE | c.3218C>T|p.Pro1073Leu |
S199 |
9 | BAA01g11870 | A01 | 5558638 | G | A | missense_variant | MODERATE | c.1622C>T|p.Pro541Leu |
S268 |
10 | BAA01g11870 | A01 | 5559140 | G | A | synonymous_variant | LOW | c.1236C>T|p.Ile412Ile |
S178 S198 |
11 | BAA01g11870 | A01 | 5559603 | C | T | missense_variant | MODERATE | c.773G>A|p.Arg258Gln |
S303 |
12 | BAA01g11870 | A01 | 5560750 | G | A | upstream_gene_variant | MODIFIER | c.-263C>T| |
S11 |
13 | BAA01g11870 | A01 | 5562054 | G | A | upstream_gene_variant | MODIFIER | c.-1567C>T| |
S186 |
14 | BAA01g11870 | A01 | 5562080 | C | T | upstream_gene_variant | MODIFIER | c.-1593G>A| |
S171 |