Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g02800 | A10 | 1341902 | G | A | upstream_gene_variant | MODIFIER | c.-368G>A| |
S245 |
2 | BAA10g02800 | A10 | 1342300 | G | A | missense_variant | MODERATE | c.31G>A|p.Asp11Asn |
S38 |
3 | BAA10g02800 | A10 | 1342333 | C | T | missense_variant | MODERATE | c.64C>T|p.Pro22Ser |
S73 S91 |
4 | BAA10g02800 | A10 | 1342787 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.285-1G>A| |
S189 |
5 | BAA10g02800 | A10 | 1343091 | C | T | missense_variant | MODERATE | c.499C>T|p.Leu167Phe |
S273 |
6 | BAA10g02800 | A10 | 1343828 | G | A | missense_variant | MODERATE | c.992G>A|p.Gly331Glu |
S187 |