Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g02570 | A04 | 1520513 | C | T | splice_region_variant&stop_retained_variant | LOW | c.1769G>A|p.Ter590Ter |
S267 |
2 | BAA04g02570 | A04 | 1521468 | C | T | missense_variant | MODERATE | c.1235G>A|p.Gly412Asp |
S293 |
3 | BAA04g02570 | A04 | 1522460 | G | A | missense_variant | MODERATE | c.551C>T|p.Ser184Phe |
S280 |
4 | BAA04g02570 | A04 | 1522462 | G | A | synonymous_variant | LOW | c.549C>T|p.Ile183Ile |
S138 |
5 | BAA04g02570 | A04 | 1522553 | C | T | missense_variant | MODERATE | c.458G>A|p.Gly153Asp |
S159 S243 |
6 | BAA04g02570 | A04 | 1523328 | G | A | missense_variant | MODERATE | c.191C>T|p.Ser64Phe |
S11 |
7 | BAA04g02570 | A04 | 1523940 | G | A | upstream_gene_variant | MODIFIER | c.-422C>T| |
S161 |
8 | BAA04g02570 | A04 | 1525184 | C | T | upstream_gene_variant | MODIFIER | c.-1666G>A| |
S20 |
9 | BAA04g02570 | A04 | 1527189 | T | C | upstream_gene_variant | MODIFIER | c.-3671A>G| |
S302 |
10 | BAA04g02570 | A04 | 1528312 | C | T | upstream_gene_variant | MODIFIER | c.-4794G>A| |
S46 |