Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21500 | A01 | 10664588 | C | T | upstream_gene_variant | MODIFIER | c.-4610C>T| |
S210 S225 |
2 | BAA01g21500 | A01 | 10665004 | G | A | upstream_gene_variant | MODIFIER | c.-4194G>A| |
S271 |
3 | BAA01g21500 | A01 | 10665068 | G | A | upstream_gene_variant | MODIFIER | c.-4130G>A| |
S142 |
4 | BAA01g21500 | A01 | 10665243 | G | A | upstream_gene_variant | MODIFIER | c.-3955G>A| |
S199 |
5 | BAA01g21500 | A01 | 10665674 | C | T | upstream_gene_variant | MODIFIER | c.-3524C>T| |
S25 S264 |
6 | BAA01g21500 | A01 | 10667337 | G | A | upstream_gene_variant | MODIFIER | c.-1861G>A| |
S199 |
7 | BAA01g21500 | A01 | 10668524 | C | T | upstream_gene_variant | MODIFIER | c.-674C>T| |
S200 S3 |
8 | BAA01g21500 | A01 | 10668641 | G | A | upstream_gene_variant | MODIFIER | c.-557G>A| |
S204 |
9 | BAA01g21500 | A01 | 10668649 | C | T | upstream_gene_variant | MODIFIER | c.-549C>T| |
S44 |
10 | BAA01g21500 | A01 | 10669127 | G | A | upstream_gene_variant | MODIFIER | c.-71G>A| |
S209 |
11 | BAA01g21500 | A01 | 10669201 | G | A | missense_variant | MODERATE | c.4G>A|p.Ala2Thr |
S9 |
12 | BAA01g21500 | A01 | 10669526 | C | T | missense_variant | MODERATE | c.329C>T|p.Ser110Phe |
S10 |
13 | BAA01g21500 | A01 | 10669871 | C | T | missense_variant | MODERATE | c.479C>T|p.Pro160Leu |
S255 |
14 | BAA01g21500 | A01 | 10669921 | G | A | missense_variant | MODERATE | c.529G>A|p.Gly177Ser |
S57 |
15 | BAA01g21500 | A01 | 10671186 | C | T | downstream_gene_variant | MODIFIER | c.*1116C>T| |
S143 |
16 | BAA01g21500 | A01 | 10671191 | C | T | downstream_gene_variant | MODIFIER | c.*1121C>T| |
S42 |
17 | BAA01g21500 | A01 | 10672847 | C | T | downstream_gene_variant | MODIFIER | c.*2777C>T| |
S146 |
18 | BAA01g21500 | A01 | 10673094 | G | A | downstream_gene_variant | MODIFIER | c.*3024G>A| |
S13 |
19 | BAA01g21500 | A01 | 10673444 | G | A | downstream_gene_variant | MODIFIER | c.*3374G>A| |
S144 |