Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g13140 | A05 | 6791989 | C | T | downstream_gene_variant | MODIFIER | c.*1773G>A| |
S55 |
2 | BAA05g13140 | A05 | 6792044 | G | A | downstream_gene_variant | MODIFIER | c.*1718C>T| |
S176 |
3 | BAA05g13140 | A05 | 6792956 | C | T | downstream_gene_variant | MODIFIER | c.*806G>A| |
S65 |
4 | BAA05g13140 | A05 | 6793814 | C | T | missense_variant | MODERATE | c.782G>A|p.Arg261Lys |
S266 |
5 | BAA05g13140 | A05 | 6794026 | G | A | synonymous_variant | LOW | c.570C>T|p.Thr190Thr |
S90 |
6 | BAA05g13140 | A05 | 6794338 | G | T | synonymous_variant | LOW | c.258C>A|p.Leu86Leu |
S217 S248 |
7 | BAA05g13140 | A05 | 6794339 | A | G | missense_variant | MODERATE | c.257T>C|p.Leu86Pro |
S217 S248 |
8 | BAA05g13140 | A05 | 6794794 | C | G | upstream_gene_variant | MODIFIER | c.-199G>C| |
S306 |
9 | BAA05g13140 | A05 | 6794826 | C | T | upstream_gene_variant | MODIFIER | c.-231G>A| |
S233 |
10 | BAA05g13140 | A05 | 6795326 | C | T | upstream_gene_variant | MODIFIER | c.-731G>A| |
S198 |
11 | BAA05g13140 | A05 | 6796266 | C | T | upstream_gene_variant | MODIFIER | c.-1671G>A| |
S19 |
12 | BAA05g13140 | A05 | 6796356 | C | T | upstream_gene_variant | MODIFIER | c.-1761G>A| |
S287 |
13 | BAA05g13140 | A05 | 6796980 | C | T | upstream_gene_variant | MODIFIER | c.-2385G>A| |
S76 |
14 | BAA05g13140 | A05 | 6797428 | C | T | upstream_gene_variant | MODIFIER | c.-2833G>A| |
S36 |
15 | BAA05g13140 | A05 | 6798479 | G | A | upstream_gene_variant | MODIFIER | c.-3884C>T| |
S296 |
16 | BAA05g13140 | A05 | 6798812 | G | A | upstream_gene_variant | MODIFIER | c.-4217C>T| |
S278 |