Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05860 | A02 | 2497523 | G | A | missense_variant | MODERATE | c.827C>T|p.Ala276Val |
S210 S225 |
2 | BAA02g05860 | A02 | 2497863 | G | A | splice_region_variant&intron_variant | LOW | c.568-5C>T| |
S210 |
3 | BAA02g05860 | A02 | 2498486 | G | A | synonymous_variant | LOW | c.199C>T|p.Leu67Leu |
S166 |
4 | BAA02g05860 | A02 | 2498571 | C | T | synonymous_variant | LOW | c.114G>A|p.Glu38Glu |
S212 |
5 | BAA02g05860 | A02 | 2498694 | C | T | missense_variant | MODERATE | c.89G>A|p.Arg30Lys |
S260 |
6 | BAA02g05860 | A02 | 2499245 | C | T | upstream_gene_variant | MODIFIER | c.-463G>A| |
S13 |
7 | BAA02g05860 | A02 | 2499271 | G | A | upstream_gene_variant | MODIFIER | c.-489C>T| |
S113 |
8 | BAA02g05860 | A02 | 2499311 | G | A | upstream_gene_variant | MODIFIER | c.-529C>T| |
S210 |
9 | BAA02g05860 | A02 | 2499523 | C | T | upstream_gene_variant | MODIFIER | c.-741G>A| |
S97 |
10 | BAA02g05860 | A02 | 2499617 | G | A | upstream_gene_variant | MODIFIER | c.-835C>T| |
S281 |
11 | BAA02g05860 | A02 | 2499864 | C | T | upstream_gene_variant | MODIFIER | c.-1082G>A| |
S295 |
12 | BAA02g05860 | A02 | 2499924 | G | A | upstream_gene_variant | MODIFIER | c.-1142C>T| |
S237 |
13 | BAA02g05860 | A02 | 2501257 | C | T | upstream_gene_variant | MODIFIER | c.-2475G>A| |
S275 |
14 | BAA02g05860 | A02 | 2502324 | G | A | upstream_gene_variant | MODIFIER | c.-3542C>T| |
S187 |
15 | BAA02g05860 | A02 | 2503093 | G | A | upstream_gene_variant | MODIFIER | c.-4311C>T| |
S23 |
16 | BAA02g05860 | A02 | 2503571 | A | T | upstream_gene_variant | MODIFIER | c.-4789T>A| |
S64 |
17 | BAA02g05860 | A02 | 2503620 | C | T | upstream_gene_variant | MODIFIER | c.-4838G>A| |
S182 |
18 | BAA02g05860 | A02 | 2503685 | G | A | upstream_gene_variant | MODIFIER | c.-4903C>T| |
S237 |