Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g11570 | A01 | 5355923 | G | A | synonymous_variant | LOW | c.2121C>T|p.Ser707Ser |
S296 |
2 | BAA01g11570 | A01 | 5356620 | C | T | missense_variant | MODERATE | c.1516G>A|p.Ala506Thr |
S67 |
3 | BAA01g11570 | A01 | 5356823 | G | A | missense_variant | MODERATE | c.1313C>T|p.Ser438Phe |
S218 |
4 | BAA01g11570 | A01 | 5356874 | G | A | missense_variant | MODERATE | c.1262C>T|p.Ala421Val |
S294 |
5 | BAA01g11570 | A01 | 5357229 | C | T | missense_variant | MODERATE | c.907G>A|p.Ala303Thr |
S177 |
6 | BAA01g11570 | A01 | 5357550 | C | T | missense_variant | MODERATE | c.586G>A|p.Glu196Lys |
S260 |
7 | BAA01g11570 | A01 | 5357888 | C | T | missense_variant | MODERATE | c.248G>A|p.Gly83Glu |
S303 |
8 | BAA01g11570 | A01 | 5357962 | G | A | synonymous_variant | LOW | c.174C>T|p.Leu58Leu |
S57 |
9 | BAA01g11570 | A01 | 5358060 | C | T | missense_variant | MODERATE | c.76G>A|p.Gly26Ser |
S265 |
10 | BAA01g11570 | A01 | 5358089 | C | T | missense_variant | MODERATE | c.47G>A|p.Gly16Glu |
S170 |
11 | BAA01g11570 | A01 | 5358355 | C | T | upstream_gene_variant | MODIFIER | c.-220G>A| |
S265 |
12 | BAA01g11570 | A01 | 5361227 | C | T | upstream_gene_variant | MODIFIER | c.-3092G>A| |
S303 |
13 | BAA01g11570 | A01 | 5361856 | G | A | upstream_gene_variant | MODIFIER | c.-3721C>T| |
S232 |
14 | BAA01g11570 | A01 | 5361975 | G | A | upstream_gene_variant | MODIFIER | c.-3840C>T| |
S241 |