Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00950 | A09 | 697019 | G | A | missense_variant | MODERATE | c.1229C>T|p.Ser410Phe |
S28 |
2 | BAA09g00950 | A09 | 697049 | G | A | missense_variant | MODERATE | c.1199C>T|p.Ala400Val |
S187 |
3 | BAA09g00950 | A09 | 697313 | G | A | intron_variant | MODIFIER | c.965-30C>T| |
S164 |
4 | BAA09g00950 | A09 | 698889 | G | A | upstream_gene_variant | MODIFIER | c.-506C>T| |
S36 |
5 | BAA09g00950 | A09 | 699653 | C | T | upstream_gene_variant | MODIFIER | c.-1270G>A| |
S297 |
6 | BAA09g00950 | A09 | 701211 | C | T | upstream_gene_variant | MODIFIER | c.-2828G>A| |
S239 |
7 | BAA09g00950 | A09 | 701813 | C | T | upstream_gene_variant | MODIFIER | c.-3430G>A| |
S247 |
8 | BAA09g00950 | A09 | 702501 | C | T | upstream_gene_variant | MODIFIER | c.-4118G>A| |
S247 |
9 | BAA09g00950 | A09 | 703085 | G | A | upstream_gene_variant | MODIFIER | c.-4702C>T| |
S164 |