Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47560 | A02 | 38301024 | C | T | upstream_gene_variant | MODIFIER | c.-3776C>T| |
S216 |
2 | BAA02g47560 | A02 | 38301691 | C | T | upstream_gene_variant | MODIFIER | c.-3109C>T| |
S205 |
3 | BAA02g47560 | A02 | 38303015 | C | T | upstream_gene_variant | MODIFIER | c.-1785C>T| |
S123 |
4 | BAA02g47560 | A02 | 38303194 | C | T | upstream_gene_variant | MODIFIER | c.-1606C>T| |
S112 S250 |
5 | BAA02g47560 | A02 | 38303290 | C | T | upstream_gene_variant | MODIFIER | c.-1510C>T| |
S241 |
6 | BAA02g47560 | A02 | 38304168 | G | A | upstream_gene_variant | MODIFIER | c.-632G>A| |
S302 |
7 | BAA02g47560 | A02 | 38304900 | C | T | missense_variant | MODERATE | c.101C>T|p.Thr34Ile |
S252 |
8 | BAA02g47560 | A02 | 38305074 | G | A | missense_variant | MODERATE | c.275G>A|p.Gly92Asp |
S125 |
9 | BAA02g47560 | A02 | 38305146 | G | A | missense_variant | MODERATE | c.347G>A|p.Gly116Asp |
S200 S261 S274 |
10 | BAA02g47560 | A02 | 38306100 | G | A | downstream_gene_variant | MODIFIER | c.*677G>A| |
S282 |
11 | BAA02g47560 | A02 | 38306206 | G | A | downstream_gene_variant | MODIFIER | c.*783G>A| |
S299 |
12 | BAA02g47560 | A02 | 38306701 | C | T | downstream_gene_variant | MODIFIER | c.*1278C>T| |
S144 |
13 | BAA02g47560 | A02 | 38307266 | G | A | downstream_gene_variant | MODIFIER | c.*1843G>A| |
S264 |
14 | BAA02g47560 | A02 | 38308554 | C | T | downstream_gene_variant | MODIFIER | c.*3131C>T| |
S218 |