Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g51870 | A09 | 53957095 | C | T | missense_variant | MODERATE | c.64C>T|p.Leu22Phe |
S242 |
2 | BAA09g51870 | A09 | 53964745 | C | T | intron_variant | MODIFIER | c.3315+1610C>T| |
S278 |
3 | BAA09g51870 | A09 | 53964862 | C | T | intron_variant | MODIFIER | c.3316-1517C>T| |
S250 |
4 | BAA09g51870 | A09 | 53966669 | C | T | intron_variant | MODIFIER | c.3507+13C>T| |
S100 |
5 | BAA09g51870 | A09 | 53967307 | C | T | intron_variant | MODIFIER | c.3873+41C>T| |
S205 |
6 | BAA09g51870 | A09 | 53967449 | C | T | intron_variant | MODIFIER | c.3936+11C>T| |
S121 |