Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g32980 | A08 | 21609571 | C | T | missense_variant | MODERATE | c.2618G>A|p.Gly873Glu |
S249 |
2 | BAA08g32980 | A08 | 21609577 | G | A | missense_variant | MODERATE | c.2612C>T|p.Ser871Leu |
S69 |
3 | BAA08g32980 | A08 | 21609797 | G | A | missense_variant | MODERATE | c.2480C>T|p.Ala827Val |
S56 |
4 | BAA08g32980 | A08 | 21610234 | G | A | missense_variant | MODERATE | c.2207C>T|p.Ser736Phe |
S139 |
5 | BAA08g32980 | A08 | 21610601 | G | A | missense_variant | MODERATE | c.2150C>T|p.Ser717Phe |
S276 |
6 | BAA08g32980 | A08 | 21612711 | C | T | missense_variant | MODERATE | c.1358G>A|p.Gly453Asp |
S45 |
7 | BAA08g32980 | A08 | 21614423 | C | T | synonymous_variant | LOW | c.573G>A|p.Lys191Lys |
S61 |
8 | BAA08g32980 | A08 | 21615022 | G | A | missense_variant | MODERATE | c.394C>T|p.Leu132Phe |
S200 |
9 | BAA08g32980 | A08 | 21615405 | C | T | missense_variant | MODERATE | c.173G>A|p.Ser58Asn |
S206 S26 |
10 | BAA08g32980 | A08 | 21616134 | C | T | upstream_gene_variant | MODIFIER | c.-445G>A| |
S201 |
11 | BAA08g32980 | A08 | 21616464 | G | A | upstream_gene_variant | MODIFIER | c.-775C>T| |
S182 |
12 | BAA08g32980 | A08 | 21616527 | G | A | upstream_gene_variant | MODIFIER | c.-838C>T| |
S260 |
13 | BAA08g32980 | A08 | 21616643 | G | A | upstream_gene_variant | MODIFIER | c.-954C>T| |
S297 |
14 | BAA08g32980 | A08 | 21616702 | G | A | upstream_gene_variant | MODIFIER | c.-1013C>T| |
S35 |
15 | BAA08g32980 | A08 | 21618965 | G | A | upstream_gene_variant | MODIFIER | c.-3276C>T| |
S40 S49 |