Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g18250 | A09 | 10944622 | C | T | missense_variant | MODERATE | c.1052G>A|p.Gly351Glu |
S115 |
2 | BAA09g18250 | A09 | 10944827 | C | T | missense_variant | MODERATE | c.847G>A|p.Glu283Lys |
S224 |
3 | BAA09g18250 | A09 | 10944854 | C | T | missense_variant | MODERATE | c.820G>A|p.Glu274Lys |
S132 S137 S215 |
4 | BAA09g18250 | A09 | 10945186 | C | T | missense_variant | MODERATE | c.488G>A|p.Ser163Asn |
S19 |
5 | BAA09g18250 | A09 | 10945351 | G | A | missense_variant | MODERATE | c.323C>T|p.Ser108Phe |
S301 S304 |
6 | BAA09g18250 | A09 | 10946567 | C | T | upstream_gene_variant | MODIFIER | c.-894G>A| |
S161 |
7 | BAA09g18250 | A09 | 10946685 | T | G | upstream_gene_variant | MODIFIER | c.-1012A>C| |
S160 S184 S228 S40 |
8 | BAA09g18250 | A09 | 10947710 | G | A | upstream_gene_variant | MODIFIER | c.-2037C>T| |
S152 |
9 | BAA09g18250 | A09 | 10949571 | G | A | upstream_gene_variant | MODIFIER | c.-3898C>T| |
S95 |
10 | BAA09g18250 | A09 | 10950635 | G | A | upstream_gene_variant | MODIFIER | c.-4962C>T| |
S205 |