Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g06620 | A05 | 3205296 | G | A | upstream_gene_variant | MODIFIER | c.-250G>A| |
S67 |
2 | BAA05g06620 | A05 | 3205575 | C | T | synonymous_variant | LOW | c.30C>T|p.Leu10Leu |
S264 |
3 | BAA05g06620 | A05 | 3205865 | C | T | missense_variant | MODERATE | c.320C>T|p.Pro107Leu |
S56 |
4 | BAA05g06620 | A05 | 3207005 | G | A | missense_variant | MODERATE | c.824G>A|p.Gly275Asp |
S202 |
5 | BAA05g06620 | A05 | 3207053 | C | T | missense_variant | MODERATE | c.872C>T|p.Ser291Phe |
S295 |
6 | BAA05g06620 | A05 | 3207312 | C | T | missense_variant | MODERATE | c.1067C>T|p.Ala356Val |
S62 |
7 | BAA05g06620 | A05 | 3207778 | C | T | splice_region_variant&intron_variant | LOW | c.1259-4C>T| |
S18 |
8 | BAA05g06620 | A05 | 3208203 | G | A | splice_region_variant&intron_variant | LOW | c.1419-7G>A| |
S34 |
9 | BAA05g06620 | A05 | 3209093 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1878-1G>A| |
S156 |
10 | BAA05g06620 | A05 | 3209284 | C | T | missense_variant | MODERATE | c.2068C>T|p.Arg690Cys |
S87 |