Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44440 | A01 | 29533755 | C | T | downstream_gene_variant | MODIFIER | c.*1202G>A| |
S267 |
2 | BAA01g44440 | A01 | 29535150 | G | A | missense_variant | MODERATE | c.3043C>T|p.Arg1015Cys |
S98 |
3 | BAA01g44440 | A01 | 29535846 | G | A | splice_region_variant&intron_variant | LOW | c.2506-4C>T| |
S297 |
4 | BAA01g44440 | A01 | 29536860 | C | T | missense_variant | MODERATE | c.2116G>A|p.Asp706Asn |
S125 |
5 | BAA01g44440 | A01 | 29537564 | C | T | missense_variant | MODERATE | c.1639G>A|p.Ala547Thr |
S251 |
6 | BAA01g44440 | A01 | 29537993 | G | A | synonymous_variant | LOW | c.1398C>T|p.Phe466Phe |
S180 |
7 | BAA01g44440 | A01 | 29538217 | C | T | missense_variant&splice_region_variant | MODERATE | c.1174G>A|p.Val392Ile |
S233 |
8 | BAA01g44440 | A01 | 29538700 | C | T | missense_variant | MODERATE | c.892G>A|p.Glu298Lys |
S205 |
9 | BAA01g44440 | A01 | 29538866 | C | T | missense_variant | MODERATE | c.808G>A|p.Glu270Lys |
S189 |
10 | BAA01g44440 | A01 | 29539009 | G | A | missense_variant | MODERATE | c.665C>T|p.Ser222Phe |
S108 |
11 | BAA01g44440 | A01 | 29539678 | C | T | synonymous_variant | LOW | c.327G>A|p.Lys109Lys |
S282 |
12 | BAA01g44440 | A01 | 29540803 | C | T | upstream_gene_variant | MODIFIER | c.-646G>A| |
S191 |
13 | BAA01g44440 | A01 | 29542965 | C | T | upstream_gene_variant | MODIFIER | c.-2808G>A| |
S112 |
14 | BAA01g44440 | A01 | 29543454 | C | T | upstream_gene_variant | MODIFIER | c.-3297G>A| |
S204 |
15 | BAA01g44440 | A01 | 29544818 | C | T | upstream_gene_variant | MODIFIER | c.-4661G>A| |
S235 |