Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g33230 | A05 | 35038892 | C | T | missense_variant | MODERATE | c.3190G>A|p.Glu1064Lys |
S202 |
2 | BAA05g33230 | A05 | 35042538 | C | T | missense_variant | MODERATE | c.1342G>A|p.Val448Ile |
S115 |
3 | BAA05g33230 | A05 | 35044329 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.781-1G>A| |
S47 |
4 | BAA05g33230 | A05 | 35044810 | C | T | missense_variant | MODERATE | c.766G>A|p.Asp256Asn |
S73 S91 |
5 | BAA05g33230 | A05 | 35044824 | G | A | missense_variant | MODERATE | c.752C>T|p.Ala251Val |
S219 S72 |
6 | BAA05g33230 | A05 | 35045856 | C | T | missense_variant | MODERATE | c.302G>A|p.Gly101Asp |
S45 |
7 | BAA05g33230 | A05 | 35047432 | C | T | upstream_gene_variant | MODIFIER | c.-1064G>A| |
S288 |
8 | BAA05g33230 | A05 | 35047707 | G | A | upstream_gene_variant | MODIFIER | c.-1339C>T| |
S221 |