Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g22860 | A07 | 27000970 | C | T | missense_variant | MODERATE | c.28C>T|p.His10Tyr |
S217 S248 |
2 | BAA07g22860 | A07 | 27002552 | G | A | synonymous_variant | LOW | c.588G>A|p.Leu196Leu |
S11 |
3 | BAA07g22860 | A07 | 27003448 | C | T | missense_variant | MODERATE | c.1133C>T|p.Pro378Leu |
S250 |
4 | BAA07g22860 | A07 | 27004241 | C | T | missense_variant | MODERATE | c.1477C>T|p.Leu493Phe |
S162 |
5 | BAA07g22860 | A07 | 27005004 | C | T | synonymous_variant | LOW | c.1662C>T|p.Tyr554Tyr |
S17 |
6 | BAA07g22860 | A07 | 27005150 | G | A | missense_variant | MODERATE | c.1808G>A|p.Gly603Asp |
S80 |
7 | BAA07g22860 | A07 | 27005577 | C | T | synonymous_variant | LOW | c.2013C>T|p.Ile671Ile |
S152 |
8 | BAA07g22860 | A07 | 27006368 | G | A | missense_variant | MODERATE | c.2438G>A|p.Gly813Glu |
S185 |
9 | BAA07g22860 | A07 | 27007623 | C | T | synonymous_variant | LOW | c.3255C>T|p.Asp1085Asp |
S206 |