Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g64670 | A09 | 59908572 | C | T | missense_variant | MODERATE | c.2470G>A|p.Asp824Asn |
S26 |
2 | BAA09g64670 | A09 | 59909391 | G | A | splice_region_variant&intron_variant | LOW | c.1811-7C>T| |
S189 |
3 | BAA09g64670 | A09 | 59911237 | G | A | missense_variant | MODERATE | c.293C>T|p.Ser98Phe |
S128 |
4 | BAA09g64670 | A09 | 59911383 | G | A | synonymous_variant | LOW | c.147C>T|p.Phe49Phe |
S17 |
5 | BAA09g64670 | A09 | 59911429 | G | A | missense_variant | MODERATE | c.101C>T|p.Thr34Ile |
S209 |
6 | BAA09g64670 | A09 | 59911475 | G | A | missense_variant | MODERATE | c.55C>T|p.Leu19Phe |
S262 |
7 | BAA09g64670 | A09 | 59913018 | C | T | upstream_gene_variant | MODIFIER | c.-1489G>A| |
S241 |
8 | BAA09g64670 | A09 | 59914133 | G | A | upstream_gene_variant | MODIFIER | c.-2604C>T| |
S197 |
9 | BAA09g64670 | A09 | 59915483 | C | T | upstream_gene_variant | MODIFIER | c.-3954G>A| |
S303 |
10 | BAA09g64670 | A09 | 59915485 | C | T | upstream_gene_variant | MODIFIER | c.-3956G>A| |
S20 |
11 | BAA09g64670 | A09 | 59915673 | C | T | upstream_gene_variant | MODIFIER | c.-4144G>A| |
S241 |