Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21940 | A01 | 10918041 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.328-1G>A| |
S287 |
2 | BAA01g21940 | A01 | 10919080 | C | T | missense_variant | MODERATE | c.823C>T|p.Leu275Phe |
S38 |
3 | BAA01g21940 | A01 | 10920068 | C | T | missense_variant | MODERATE | c.1214C>T|p.Pro405Leu |
S134 |
4 | BAA01g21940 | A01 | 10920411 | C | T | splice_region_variant&intron_variant | LOW | c.1321-4C>T| |
S182 |
5 | BAA01g21940 | A01 | 10921901 | G | A | missense_variant | MODERATE | c.1880G>A|p.Arg627Lys |
S123 |
6 | BAA01g21940 | A01 | 10923307 | G | A | intron_variant | MODIFIER | c.2368+75G>A| |
S244 |
7 | BAA01g21940 | A01 | 10923553 | C | T | missense_variant | MODERATE | c.2380C>T|p.Pro794Ser |
S280 |
8 | BAA01g21940 | A01 | 10924516 | C | T | missense_variant | MODERATE | c.2705C>T|p.Ser902Leu |
S8 |
9 | BAA01g21940 | A01 | 10925072 | C | T | missense_variant | MODERATE | c.2897C>T|p.Pro966Leu |
S256 |
10 | BAA01g21940 | A01 | 10925562 | G | A | missense_variant | MODERATE | c.3092G>A|p.Gly1031Glu |
S232 |
11 | BAA01g21940 | A01 | 10925636 | A | G | missense_variant | MODERATE | c.3166A>G|p.Ile1056Val |
S232 |
12 | BAA01g21940 | A01 | 10926001 | C | T | synonymous_variant | LOW | c.3336C>T|p.Ala1112Ala |
S247 |
13 | BAA01g21940 | A01 | 10926688 | G | A | synonymous_variant | LOW | c.3846G>A|p.Glu1282Glu |
S73 |
14 | BAA01g21940 | A01 | 10928713 | C | T | synonymous_variant | LOW | c.5235C>T|p.Val1745Val |
S303 |
15 | BAA01g21940 | A01 | 10933133 | G | A | downstream_gene_variant | MODIFIER | c.*4180G>A| |
S71 |
16 | BAA01g21940 | A01 | 10933348 | G | A | downstream_gene_variant | MODIFIER | c.*4395G>A| |
S271 |