Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g19250 | A09 | 11696126 | C | T | upstream_gene_variant | MODIFIER | c.-3791C>T| |
S128 S138 S237 S288 |
2 | BAA09g19250 | A09 | 11697660 | C | T | upstream_gene_variant | MODIFIER | c.-2257C>T| |
S283 |
3 | BAA09g19250 | A09 | 11699384 | C | T | upstream_gene_variant | MODIFIER | c.-533C>T| |
S5 |
4 | BAA09g19250 | A09 | 11699433 | G | A | upstream_gene_variant | MODIFIER | c.-484G>A| |
S201 |
5 | BAA09g19250 | A09 | 11699505 | C | T | upstream_gene_variant | MODIFIER | c.-412C>T| |
S255 S69 |
6 | BAA09g19250 | A09 | 11699755 | G | A | upstream_gene_variant | MODIFIER | c.-162G>A| |
S180 |
7 | BAA09g19250 | A09 | 11699893 | C | T | upstream_gene_variant | MODIFIER | c.-24C>T| |
S64 |
8 | BAA09g19250 | A09 | 11700209 | C | T | synonymous_variant | LOW | c.219C>T|p.Val73Val |
S289 S290 |
9 | BAA09g19250 | A09 | 11700278 | G | A | stop_gained | HIGH | c.288G>A|p.Trp96* |
S74 |
10 | BAA09g19250 | A09 | 11702776 | G | A | missense_variant | MODERATE | c.922G>A|p.Val308Ile |
S32 |
11 | BAA09g19250 | A09 | 11703205 | C | T | missense_variant | MODERATE | c.1067C>T|p.Pro356Leu |
S116 |
12 | BAA09g19250 | A09 | 11703329 | C | T | synonymous_variant | LOW | c.1191C>T|p.Arg397Arg |
S274 S303 |
13 | BAA09g19250 | A09 | 11705134 | C | T | missense_variant | MODERATE | c.2344C>T|p.Pro782Ser |
S104 S52 |
14 | BAA09g19250 | A09 | 11705188 | G | A | missense_variant | MODERATE | c.2398G>A|p.Val800Met |
S142 |
15 | BAA09g19250 | A09 | 11705329 | G | A | missense_variant | MODERATE | c.2539G>A|p.Val847Met |
S209 |