Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g20220 | A09 | 12475527 | C | T | missense_variant | MODERATE | c.2684G>A|p.Gly895Glu |
S9 |
2 | BAA09g20220 | A09 | 12475567 | G | A | missense_variant | MODERATE | c.2644C>T|p.Pro882Ser |
S126 |
3 | BAA09g20220 | A09 | 12475629 | C | T | missense_variant | MODERATE | c.2582G>A|p.Arg861Lys |
S55 |
4 | BAA09g20220 | A09 | 12475852 | G | A | missense_variant | MODERATE | c.2359C>T|p.Pro787Ser |
S115 |
5 | BAA09g20220 | A09 | 12475875 | G | A | missense_variant | MODERATE | c.2336C>T|p.Pro779Leu |
S208 S219 |
6 | BAA09g20220 | A09 | 12476373 | G | A | intron_variant | MODIFIER | c.2037-22C>T| |
S301 S304 |
7 | BAA09g20220 | A09 | 12477064 | G | A | missense_variant | MODERATE | c.1720C>T|p.Pro574Ser |
S194 |
8 | BAA09g20220 | A09 | 12477462 | C | T | intron_variant | MODIFIER | c.1586+17G>A| |
S245 |
9 | BAA09g20220 | A09 | 12477754 | G | A | intron_variant | MODIFIER | c.1457+38C>T| |
S122 |
10 | BAA09g20220 | A09 | 12477770 | C | T | intron_variant | MODIFIER | c.1457+22G>A| |
S115 |
11 | BAA09g20220 | A09 | 12479606 | C | T | missense_variant | MODERATE | c.902G>A|p.Arg301Gln |
S128 |
12 | BAA09g20220 | A09 | 12479765 | G | A | missense_variant | MODERATE | c.856C>T|p.Pro286Ser |
S122 |
13 | BAA09g20220 | A09 | 12480677 | C | T | missense_variant | MODERATE | c.308G>A|p.Arg103Lys |
S295 |
14 | BAA09g20220 | A09 | 12482570 | G | A | upstream_gene_variant | MODIFIER | c.-1303C>T| |
S233 |
15 | BAA09g20220 | A09 | 12482599 | G | A | upstream_gene_variant | MODIFIER | c.-1332C>T| |
S185 |
16 | BAA09g20220 | A09 | 12482997 | G | A | upstream_gene_variant | MODIFIER | c.-1730C>T| |
S130 |
17 | BAA09g20220 | A09 | 12483766 | C | T | upstream_gene_variant | MODIFIER | c.-2499G>A| |
S132 S137 S215 S89 |
18 | BAA09g20220 | A09 | 12485749 | G | A | upstream_gene_variant | MODIFIER | c.-4482C>T| |
S178 |
19 | BAA09g20220 | A09 | 12485807 | C | T | upstream_gene_variant | MODIFIER | c.-4540G>A| |
S204 |
20 | BAA09g20220 | A09 | 12486257 | C | T | upstream_gene_variant | MODIFIER | c.-4990G>A| |
S103 |