Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g21780 | A03 | 9848439 | G | A | synonymous_variant | LOW | c.273G>A|p.Val91Val |
S188 |
2 | BAA03g21780 | A03 | 9848522 | G | A | splice_region_variant&intron_variant | LOW | c.349+7G>A| |
S132 S215 |
3 | BAA03g21780 | A03 | 9848742 | G | A | intron_variant | MODIFIER | c.349+227G>A| |
S202 |
4 | BAA03g21780 | A03 | 9849502 | G | A | synonymous_variant | LOW | c.651G>A|p.Leu217Leu |
S283 |
5 | BAA03g21780 | A03 | 9851059 | G | A | missense_variant | MODERATE | c.1370G>A|p.Gly457Glu |
S51 |
6 | BAA03g21780 | A03 | 9851189 | C | T | synonymous_variant | LOW | c.1408C>T|p.Leu470Leu |
S171 |
7 | BAA03g21780 | A03 | 9851318 | C | T | missense_variant | MODERATE | c.1537C>T|p.Pro513Ser |
S232 |
8 | BAA03g21780 | A03 | 9851334 | G | A | missense_variant | MODERATE | c.1553G>A|p.Arg518His |
S198 |
9 | BAA03g21780 | A03 | 9852177 | C | T | missense_variant | MODERATE | c.1777C>T|p.Pro593Ser |
S187 |
10 | BAA03g21780 | A03 | 9852922 | C | T | synonymous_variant | LOW | c.2082C>T|p.Ile694Ile |
S116 |
11 | BAA03g21780 | A03 | 9853041 | C | T | missense_variant | MODERATE | c.2201C>T|p.Ser734Phe |
S112 |