Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g08080 | A04 | 5496889 | C | T | downstream_gene_variant | MODIFIER | c.*2399G>A| |
S139 |
2 | BAA04g08080 | A04 | 5499664 | C | T | missense_variant | MODERATE | c.1457G>A|p.Gly486Asp |
S79 S84 |
3 | BAA04g08080 | A04 | 5499797 | C | T | missense_variant | MODERATE | c.1324G>A|p.Gly442Ser |
S98 |
4 | BAA04g08080 | A04 | 5499810 | C | T | synonymous_variant | LOW | c.1311G>A|p.Leu437Leu |
S115 |
5 | BAA04g08080 | A04 | 5500146 | C | T | synonymous_variant | LOW | c.975G>A|p.Val325Val |
S167 |
6 | BAA04g08080 | A04 | 5500964 | C | T | missense_variant | MODERATE | c.157G>A|p.Val53Met |
S302 |
7 | BAA04g08080 | A04 | 5500966 | C | T | missense_variant | MODERATE | c.155G>A|p.Gly52Glu |
S172 S217 |
8 | BAA04g08080 | A04 | 5501540 | C | T | missense_variant | MODERATE | c.4G>A|p.Val2Ile |
S263 |
9 | BAA04g08080 | A04 | 5502028 | C | T | upstream_gene_variant | MODIFIER | c.-485G>A| |
S7 |
10 | BAA04g08080 | A04 | 5503650 | G | A | upstream_gene_variant | MODIFIER | c.-2107C>T| |
S62 |
11 | BAA04g08080 | A04 | 5504644 | C | T | upstream_gene_variant | MODIFIER | c.-3101G>A| |
S265 |
12 | BAA04g08080 | A04 | 5505857 | C | T | upstream_gene_variant | MODIFIER | c.-4314G>A| |
S268 |
13 | BAA04g08080 | A04 | 5506034 | C | T | upstream_gene_variant | MODIFIER | c.-4491G>A| |
S6 |
14 | BAA04g08080 | A04 | 5506077 | G | A | upstream_gene_variant | MODIFIER | c.-4534C>T| |
S34 |