Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10570 | A01 | 4846950 | C | T | upstream_gene_variant | MODIFIER | c.-3249C>T| |
S167 |
2 | BAA01g10570 | A01 | 4847543 | G | A | upstream_gene_variant | MODIFIER | c.-2656G>A| |
S144 |
3 | BAA01g10570 | A01 | 4848435 | C | T | upstream_gene_variant | MODIFIER | c.-1764C>T| |
S136 |
4 | BAA01g10570 | A01 | 4848825 | C | T | upstream_gene_variant | MODIFIER | c.-1374C>T| |
S100 |
5 | BAA01g10570 | A01 | 4849147 | C | T | upstream_gene_variant | MODIFIER | c.-1052C>T| |
S62 |
6 | BAA01g10570 | A01 | 4849306 | G | A | upstream_gene_variant | MODIFIER | c.-893G>A| |
S67 |
7 | BAA01g10570 | A01 | 4849548 | C | T | upstream_gene_variant | MODIFIER | c.-651C>T| |
S296 |
8 | BAA01g10570 | A01 | 4850292 | C | T | synonymous_variant | LOW | c.94C>T|p.Leu32Leu |
S301 |
9 | BAA01g10570 | A01 | 4850374 | G | A | missense_variant | MODERATE | c.176G>A|p.Gly59Glu |
S207 |
10 | BAA01g10570 | A01 | 4850655 | G | A | missense_variant | MODERATE | c.457G>A|p.Val153Met |
S293 |
11 | BAA01g10570 | A01 | 4851515 | C | T | missense_variant | MODERATE | c.1231C>T|p.Pro411Ser |
S203 |
12 | BAA01g10570 | A01 | 4854040 | C | T | downstream_gene_variant | MODIFIER | c.*2436C>T| |
S151 |
13 | BAA01g10570 | A01 | 4854283 | G | A | downstream_gene_variant | MODIFIER | c.*2679G>A| |
S85 |
14 | BAA01g10570 | A01 | 4855461 | G | A | downstream_gene_variant | MODIFIER | c.*3857G>A| |
S259 |
15 | BAA01g10570 | A01 | 4855708 | C | T | downstream_gene_variant | MODIFIER | c.*4104C>T| |
S249 |
16 | BAA01g10570 | A01 | 4855949 | A | G | downstream_gene_variant | MODIFIER | c.*4345A>G| |
S39 |
17 | BAA01g10570 | A01 | 4856404 | C | T | downstream_gene_variant | MODIFIER | c.*4800C>T| |
S42 |