Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g26390 | A09 | 17147226 | G | A | missense_variant | MODERATE | c.1394C>T|p.Ser465Phe |
S121 |
2 | BAA09g26390 | A09 | 17147319 | G | A | missense_variant | MODERATE | c.1301C>T|p.Ala434Val |
S172 |
3 | BAA09g26390 | A09 | 17147763 | G | A | missense_variant | MODERATE | c.1036C>T|p.Leu346Phe |
S41 |
4 | BAA09g26390 | A09 | 17149019 | G | A | intron_variant | MODIFIER | c.573+70C>T| |
S89 |
5 | BAA09g26390 | A09 | 17149477 | C | T | missense_variant | MODERATE | c.371G>A|p.Arg124Lys |
S159 S243 S299 |
6 | BAA09g26390 | A09 | 17149768 | C | T | missense_variant | MODERATE | c.80G>A|p.Gly27Glu |
S99 |
7 | BAA09g26390 | A09 | 17150140 | G | A | upstream_gene_variant | MODIFIER | c.-185C>T| |
S77 S82 |
8 | BAA09g26390 | A09 | 17150142 | C | T | upstream_gene_variant | MODIFIER | c.-187G>A| |
S143 |
9 | BAA09g26390 | A09 | 17150461 | G | A | upstream_gene_variant | MODIFIER | c.-506C>T| |
S199 |
10 | BAA09g26390 | A09 | 17151104 | C | T | upstream_gene_variant | MODIFIER | c.-1149G>A| |
S62 |
11 | BAA09g26390 | A09 | 17151108 | G | A | upstream_gene_variant | MODIFIER | c.-1153C>T| |
S38 |
12 | BAA09g26390 | A09 | 17151331 | G | A | upstream_gene_variant | MODIFIER | c.-1376C>T| |
S95 |
13 | BAA09g26390 | A09 | 17151587 | G | A | upstream_gene_variant | MODIFIER | c.-1632C>T| |
S25 |
14 | BAA09g26390 | A09 | 17151782 | G | A | upstream_gene_variant | MODIFIER | c.-1827C>T| |
S221 |
15 | BAA09g26390 | A09 | 17153402 | G | A | upstream_gene_variant | MODIFIER | c.-3447C>T| |
S204 |