Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20860 | A10 | 18564246 | G | A | missense_variant | MODERATE | c.2132C>T|p.Pro711Leu |
S1 S90 |
2 | BAA10g20860 | A10 | 18564895 | C | T | synonymous_variant | LOW | c.1794G>A|p.Arg598Arg |
S168 S219 S72 |
3 | BAA10g20860 | A10 | 18564951 | C | T | missense_variant | MODERATE | c.1738G>A|p.Gly580Arg |
S96 |
4 | BAA10g20860 | A10 | 18565694 | G | A | missense_variant | MODERATE | c.1403C>T|p.Thr468Ile |
S165 |
5 | BAA10g20860 | A10 | 18567013 | C | T | missense_variant | MODERATE | c.925G>A|p.Val309Ile |
S283 |
6 | BAA10g20860 | A10 | 18567227 | C | T | synonymous_variant | LOW | c.828G>A|p.Lys276Lys |
S308 |
7 | BAA10g20860 | A10 | 18567537 | C | T | intron_variant | MODIFIER | c.808+110G>A| |
S185 |
8 | BAA10g20860 | A10 | 18568462 | G | A | synonymous_variant | LOW | c.96C>T|p.Ser32Ser |
S64 |
9 | BAA10g20860 | A10 | 18568482 | G | A | missense_variant | MODERATE | c.76C>T|p.Leu26Phe |
S1 S90 |