Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22100 | A01 | 11013370 | C | T | missense_variant | MODERATE | c.850C>T|p.Pro284Ser |
S272 |
2 | BAA01g22100 | A01 | 11013632 | G | A | splice_region_variant&intron_variant | LOW | c.1023+6G>A| |
S173 |
3 | BAA01g22100 | A01 | 11014325 | C | T | synonymous_variant | LOW | c.1273C>T|p.Leu425Leu |
S206 S26 |
4 | BAA01g22100 | A01 | 11017943 | C | T | downstream_gene_variant | MODIFIER | c.*2843C>T| |
S128 |
5 | BAA01g22100 | A01 | 11018364 | G | A | downstream_gene_variant | MODIFIER | c.*3264G>A| |
S138 |
6 | BAA01g22100 | A01 | 11018416 | C | T | downstream_gene_variant | MODIFIER | c.*3316C>T| |
S207 S260 |
7 | BAA01g22100 | A01 | 11018920 | C | T | downstream_gene_variant | MODIFIER | c.*3820C>T| |
S26 |
8 | BAA01g22100 | A01 | 11019166 | G | A | downstream_gene_variant | MODIFIER | c.*4066G>A| |
S160 |
9 | BAA01g22100 | A01 | 11020075 | G | A | downstream_gene_variant | MODIFIER | c.*4975G>A| |
S76 |