Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g25170 | A03 | 11532284 | G | A | missense_variant | MODERATE | c.11G>A|p.Gly4Glu |
S46 |
2 | BAA03g25170 | A03 | 11532307 | C | T | missense_variant | MODERATE | c.34C>T|p.Arg12Trp |
S171 |
3 | BAA03g25170 | A03 | 11532336 | G | A | synonymous_variant | LOW | c.63G>A|p.Arg21Arg |
S143 |
4 | BAA03g25170 | A03 | 11533382 | G | A | missense_variant | MODERATE | c.973G>A|p.Ala325Thr |
S209 |
5 | BAA03g25170 | A03 | 11533550 | G | A | missense_variant | MODERATE | c.1141G>A|p.Asp381Asn |
S122 |
6 | BAA03g25170 | A03 | 11533939 | C | T | missense_variant | MODERATE | c.1400C>T|p.Ala467Val |
S266 |
7 | BAA03g25170 | A03 | 11533984 | C | T | missense_variant | MODERATE | c.1445C>T|p.Ser482Phe |
S283 |
8 | BAA03g25170 | A03 | 11534266 | C | T | missense_variant | MODERATE | c.1727C>T|p.Ala576Val |
S92 |
9 | BAA03g25170 | A03 | 11534392 | C | T | missense_variant | MODERATE | c.1853C>T|p.Ser618Phe |
S16 S268 |
10 | BAA03g25170 | A03 | 11534802 | G | A | missense_variant | MODERATE | c.2263G>A|p.Ala755Thr |
S47 |
11 | BAA03g25170 | A03 | 11534944 | G | A | missense_variant | MODERATE | c.2405G>A|p.Arg802Lys |
S95 |
12 | BAA03g25170 | A03 | 11537554 | G | A | synonymous_variant | LOW | c.3933G>A|p.Leu1311Leu |
S95 |
13 | BAA03g25170 | A03 | 11538114 | C | T | missense_variant | MODERATE | c.4493C>T|p.Ser1498Phe |
S156 S157 S163 |
14 | BAA03g25170 | A03 | 11538904 | G | A | stop_gained | HIGH | c.5204G>A|p.Trp1735* |
S164 |