Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10200 | A10 | 11974431 | C | T | upstream_gene_variant | MODIFIER | c.-4679C>T| |
S149 |
2 | BAA10g10200 | A10 | 11975200 | C | T | upstream_gene_variant | MODIFIER | c.-3910C>T| |
S133 |
3 | BAA10g10200 | A10 | 11975259 | C | T | upstream_gene_variant | MODIFIER | c.-3851C>T| |
S166 |
4 | BAA10g10200 | A10 | 11975761 | G | A | upstream_gene_variant | MODIFIER | c.-3349G>A| |
S283 |
5 | BAA10g10200 | A10 | 11976665 | G | A | upstream_gene_variant | MODIFIER | c.-2445G>A| |
S16 |
6 | BAA10g10200 | A10 | 11978188 | G | A | upstream_gene_variant | MODIFIER | c.-922G>A| |
S35 |
7 | BAA10g10200 | A10 | 11979286 | C | T | intron_variant | MODIFIER | c.163+14C>T| |
S63 |
8 | BAA10g10200 | A10 | 11979770 | C | T | missense_variant | MODERATE | c.472C>T|p.Arg158Cys |
S156 |
9 | BAA10g10200 | A10 | 11980371 | C | T | missense_variant | MODERATE | c.1073C>T|p.Ser358Phe |
S243 S299 |
10 | BAA10g10200 | A10 | 11980676 | C | T | synonymous_variant | LOW | c.1378C>T|p.Leu460Leu |
S113 |
11 | BAA10g10200 | A10 | 11980704 | G | A | missense_variant | MODERATE | c.1406G>A|p.Gly469Glu |
S178 |
12 | BAA10g10200 | A10 | 11980815 | G | A | downstream_gene_variant | MODIFIER | c.*17G>A| |
S118 |
13 | BAA10g10200 | A10 | 11981149 | C | T | downstream_gene_variant | MODIFIER | c.*351C>T| |
S11 |
14 | BAA10g10200 | A10 | 11981333 | C | T | downstream_gene_variant | MODIFIER | c.*535C>T| |
S169 |
15 | BAA10g10200 | A10 | 11982514 | G | A | downstream_gene_variant | MODIFIER | c.*1716G>A| |
S179 |
16 | BAA10g10200 | A10 | 11982777 | G | A | downstream_gene_variant | MODIFIER | c.*1979G>A| |
S172 S217 |
17 | BAA10g10200 | A10 | 11983032 | G | A | downstream_gene_variant | MODIFIER | c.*2234G>A| |
S278 |
18 | BAA10g10200 | A10 | 11983390 | G | A | downstream_gene_variant | MODIFIER | c.*2592G>A| |
S208 S219 |
19 | BAA10g10200 | A10 | 11983413 | C | T | downstream_gene_variant | MODIFIER | c.*2615C>T| |
S224 |
20 | BAA10g10200 | A10 | 11985441 | G | A | downstream_gene_variant | MODIFIER | c.*4643G>A| |
S302 |