Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g17840 | A05 | 10123431 | C | T | upstream_gene_variant | MODIFIER | c.-35C>T| |
S27 |
2 | BAA05g17840 | A05 | 10123766 | C | T | missense_variant | MODERATE | c.301C>T|p.Leu101Phe |
S10 |
3 | BAA05g17840 | A05 | 10123985 | G | A | missense_variant | MODERATE | c.520G>A|p.Val174Met |
S203 |
4 | BAA05g17840 | A05 | 10124310 | G | A | missense_variant | MODERATE | c.845G>A|p.Gly282Asp |
S107 |
5 | BAA05g17840 | A05 | 10124381 | C | T | missense_variant | MODERATE | c.916C>T|p.Pro306Ser |
S143 |
6 | BAA05g17840 | A05 | 10124592 | G | A | missense_variant | MODERATE | c.1127G>A|p.Gly376Glu |
S64 |
7 | BAA05g17840 | A05 | 10124612 | G | A | missense_variant | MODERATE | c.1147G>A|p.Ala383Thr |
S210 S225 |
8 | BAA05g17840 | A05 | 10128844 | C | T | downstream_gene_variant | MODIFIER | c.*4134C>T| |
S136 |
9 | BAA05g17840 | A05 | 10129309 | C | T | downstream_gene_variant | MODIFIER | c.*4599C>T| |
S98 |
10 | BAA05g17840 | A05 | 10129413 | C | T | downstream_gene_variant | MODIFIER | c.*4703C>T| |
S50 |
11 | BAA05g17840 | A05 | 10129442 | G | A | downstream_gene_variant | MODIFIER | c.*4732G>A| |
S156 |