Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g32790 | A03 | 15245011 | C | T | stop_gained | HIGH | c.154C>T|p.Gln52* |
S190 |
2 | BAA03g32790 | A03 | 15245832 | G | A | synonymous_variant | LOW | c.975G>A|p.Lys325Lys |
S212 |
3 | BAA03g32790 | A03 | 15245962 | G | A | missense_variant | MODERATE | c.1105G>A|p.Glu369Lys |
S2 |
4 | BAA03g32790 | A03 | 15246584 | G | A | synonymous_variant | LOW | c.1545G>A|p.Lys515Lys |
S48 |
5 | BAA03g32790 | A03 | 15246742 | G | A | missense_variant | MODERATE | c.1703G>A|p.Gly568Glu |
S144 |
6 | BAA03g32790 | A03 | 15246933 | C | T | stop_gained | HIGH | c.1894C>T|p.Gln632* |
S218 |
7 | BAA03g32790 | A03 | 15247196 | C | T | synonymous_variant | LOW | c.2157C>T|p.Phe719Phe |
S9 |
8 | BAA03g32790 | A03 | 15247644 | G | A | missense_variant | MODERATE | c.2605G>A|p.Asp869Asn |
S296 |
9 | BAA03g32790 | A03 | 15247697 | C | T | synonymous_variant | LOW | c.2658C>T|p.Leu886Leu |
S132 S137 S215 S89 |
10 | BAA03g32790 | A03 | 15247731 | C | T | stop_gained | HIGH | c.2692C>T|p.Gln898* |
S16 |
11 | BAA03g32790 | A03 | 15248747 | C | T | synonymous_variant | LOW | c.2883C>T|p.Leu961Leu |
S176 |
12 | BAA03g32790 | A03 | 15249524 | C | T | synonymous_variant | LOW | c.3276C>T|p.Ser1092Ser |
S42 |