Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g20880 | A07 | 25909614 | G | A | missense_variant | MODERATE | c.1589C>T|p.Thr530Ile |
S72 S78 |
2 | BAA07g20880 | A07 | 25909945 | G | A | missense_variant | MODERATE | c.1258C>T|p.Pro420Ser |
S183 |
3 | BAA07g20880 | A07 | 25910013 | C | T | missense_variant | MODERATE | c.1190G>A|p.Gly397Glu |
S32 |
4 | BAA07g20880 | A07 | 25910484 | C | T | missense_variant | MODERATE | c.719G>A|p.Arg240Lys |
S94 |
5 | BAA07g20880 | A07 | 25910671 | G | A | missense_variant | MODERATE | c.532C>T|p.His178Tyr |
S301 S304 |
6 | BAA07g20880 | A07 | 25910894 | C | T | synonymous_variant | LOW | c.309G>A|p.Glu103Glu |
S245 |
7 | BAA07g20880 | A07 | 25911160 | G | A | missense_variant | MODERATE | c.43C>T|p.Pro15Ser |
S38 |
8 | BAA07g20880 | A07 | 25911257 | G | A | upstream_gene_variant | MODIFIER | c.-55C>T| |
S7 |
9 | BAA07g20880 | A07 | 25911461 | G | A | upstream_gene_variant | MODIFIER | c.-259C>T| |
S268 |
10 | BAA07g20880 | A07 | 25915343 | G | A | upstream_gene_variant | MODIFIER | c.-4141C>T| |
S38 |