Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g30080 | A06 | 20504264 | C | T | upstream_gene_variant | MODIFIER | c.-4587C>T| |
S115 |
2 | BAA06g30080 | A06 | 20504433 | G | A | upstream_gene_variant | MODIFIER | c.-4418G>A| |
S61 |
3 | BAA06g30080 | A06 | 20504629 | C | T | upstream_gene_variant | MODIFIER | c.-4222C>T| |
S203 |
4 | BAA06g30080 | A06 | 20506721 | G | A | upstream_gene_variant | MODIFIER | c.-2130G>A| |
S17 |
5 | BAA06g30080 | A06 | 20506725 | G | A | upstream_gene_variant | MODIFIER | c.-2126G>A| |
S170 |
6 | BAA06g30080 | A06 | 20507806 | A | C | upstream_gene_variant | MODIFIER | c.-1045A>C| |
S125 |
7 | BAA06g30080 | A06 | 20508164 | C | T | upstream_gene_variant | MODIFIER | c.-687C>T| |
S153 |
8 | BAA06g30080 | A06 | 20508537 | G | A | upstream_gene_variant | MODIFIER | c.-314G>A| |
S217 |
9 | BAA06g30080 | A06 | 20509477 | C | T | missense_variant | MODERATE | c.419C>T|p.Ser140Phe |
S189 |
10 | BAA06g30080 | A06 | 20511643 | G | A | missense_variant | MODERATE | c.1012G>A|p.Ala338Thr |
S8 |
11 | BAA06g30080 | A06 | 20511790 | C | T | missense_variant | MODERATE | c.1159C>T|p.Pro387Ser |
S159 S243 |