Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g51500 | A09 | 53804829 | G | A | upstream_gene_variant | MODIFIER | c.-3958G>A| |
S277 |
2 | BAA09g51500 | A09 | 53805972 | G | A | upstream_gene_variant | MODIFIER | c.-2815G>A| |
S116 |
3 | BAA09g51500 | A09 | 53809154 | C | T | missense_variant | MODERATE | c.245C>T|p.Thr82Ile |
S205 |
4 | BAA09g51500 | A09 | 53809220 | C | T | missense_variant | MODERATE | c.311C>T|p.Pro104Leu |
S157 |
5 | BAA09g51500 | A09 | 53809549 | G | A | missense_variant | MODERATE | c.451G>A|p.Asp151Asn |
S166 |
6 | BAA09g51500 | A09 | 53809678 | G | A | missense_variant | MODERATE | c.493G>A|p.Gly165Arg |
S270 |
7 | BAA09g51500 | A09 | 53810056 | G | A | missense_variant | MODERATE | c.613G>A|p.Gly205Ser |
S189 |
8 | BAA09g51500 | A09 | 53810369 | C | T | missense_variant | MODERATE | c.926C>T|p.Ala309Val |
S117 |
9 | BAA09g51500 | A09 | 53811263 | C | T | missense_variant | MODERATE | c.1592C>T|p.Pro531Leu |
S295 |
10 | BAA09g51500 | A09 | 53811750 | G | A | missense_variant | MODERATE | c.1918G>A|p.Glu640Lys |
S241 |