Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g02460 | A09 | 1593797 | C | T | missense_variant | MODERATE | c.1280G>A|p.Arg427Gln |
S59 |
2 | BAA09g02460 | A09 | 1593835 | G | A | synonymous_variant | LOW | c.1242C>T|p.His414His |
S188 |
3 | BAA09g02460 | A09 | 1593985 | C | T | synonymous_variant | LOW | c.1092G>A|p.Glu364Glu |
S53 |
4 | BAA09g02460 | A09 | 1593994 | C | T | synonymous_variant | LOW | c.1083G>A|p.Val361Val |
S156 |
5 | BAA09g02460 | A09 | 1594013 | G | A | missense_variant | MODERATE | c.1064C>T|p.Pro355Leu |
S190 S223 S284 S287 S57 |
6 | BAA09g02460 | A09 | 1594274 | C | T | missense_variant | MODERATE | c.803G>A|p.Cys268Tyr |
S104 S52 |
7 | BAA09g02460 | A09 | 1594356 | C | T | missense_variant | MODERATE | c.721G>A|p.Glu241Lys |
S87 |
8 | BAA09g02460 | A09 | 1594715 | C | T | missense_variant | MODERATE | c.362G>A|p.Arg121Lys |
S270 |
9 | BAA09g02460 | A09 | 1599703 | G | A | upstream_gene_variant | MODIFIER | c.-4627C>T| |
S271 |