Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g12120 | A04 | 17937232 | C | T | upstream_gene_variant | MODIFIER | c.-3356C>T| |
S18 |
2 | BAA04g12120 | A04 | 17940601 | C | A | missense_variant | MODERATE | c.14C>A|p.Ser5Tyr |
S26 |
3 | BAA04g12120 | A04 | 17940946 | C | T | missense_variant | MODERATE | c.167C>T|p.Thr56Ile |
S64 |
4 | BAA04g12120 | A04 | 17941364 | G | A | synonymous_variant | LOW | c.585G>A|p.Ala195Ala |
S283 |
5 | BAA04g12120 | A04 | 17941463 | G | A | stop_gained | HIGH | c.684G>A|p.Trp228* |
S160 |
6 | BAA04g12120 | A04 | 17941795 | C | T | missense_variant&splice_region_variant | MODERATE | c.952C>T|p.Arg318Cys |
S6 |
7 | BAA04g12120 | A04 | 17941979 | G | A | missense_variant | MODERATE | c.1057G>A|p.Glu353Lys |
S236 |
8 | BAA04g12120 | A04 | 17942221 | G | A | missense_variant | MODERATE | c.1210G>A|p.Ala404Thr |
S142 |
9 | BAA04g12120 | A04 | 17942243 | C | T | missense_variant | MODERATE | c.1232C>T|p.Ser411Phe |
S68 |
10 | BAA04g12120 | A04 | 17943374 | A | C | downstream_gene_variant | MODIFIER | c.*589A>C| |
S119 S186 S28 |
11 | BAA04g12120 | A04 | 17943376 | A | C | downstream_gene_variant | MODIFIER | c.*591A>C| |
S119 S186 S28 |
12 | BAA04g12120 | A04 | 17943692 | C | T | downstream_gene_variant | MODIFIER | c.*907C>T| |
S265 |
13 | BAA04g12120 | A04 | 17946261 | G | A | downstream_gene_variant | MODIFIER | c.*3476G>A| |
S267 |