Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g37570 | A01 | 25099754 | C | T | upstream_gene_variant | MODIFIER | c.-4242C>T| |
S69 |
2 | BAA01g37570 | A01 | 25100573 | C | T | upstream_gene_variant | MODIFIER | c.-3423C>T| |
S23 |
3 | BAA01g37570 | A01 | 25104020 | C | T | missense_variant | MODERATE | c.25C>T|p.Pro9Ser |
S279 |
4 | BAA01g37570 | A01 | 25104108 | C | T | missense_variant | MODERATE | c.113C>T|p.Pro38Leu |
S17 |
5 | BAA01g37570 | A01 | 25104389 | G | A | missense_variant | MODERATE | c.394G>A|p.Gly132Arg |
S35 |
6 | BAA01g37570 | A01 | 25104460 | C | T | synonymous_variant | LOW | c.465C>T|p.Tyr155Tyr |
S38 |
7 | BAA01g37570 | A01 | 25104794 | G | A | missense_variant | MODERATE | c.799G>A|p.Glu267Lys |
S159 S188 S243 S276 S298 S299 |
8 | BAA01g37570 | A01 | 25104886 | C | T | synonymous_variant | LOW | c.891C>T|p.Ala297Ala |
S161 |
9 | BAA01g37570 | A01 | 25104903 | G | A | missense_variant | MODERATE | c.908G>A|p.Gly303Glu |
S91 |
10 | BAA01g37570 | A01 | 25104931 | G | A | synonymous_variant | LOW | c.936G>A|p.Gln312Gln |
S159 S243 |
11 | BAA01g37570 | A01 | 25105605 | G | A | missense_variant | MODERATE | c.1610G>A|p.Gly537Asp |
S221 |