Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g13610 | A10 | 14598337 | G | A | downstream_gene_variant | MODIFIER | c.*226C>T| |
S118 |
2 | BAA10g13610 | A10 | 14599229 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1554-1G>A| |
S79 S91 |
3 | BAA10g13610 | A10 | 14600568 | C | T | missense_variant | MODERATE | c.989G>A|p.Gly330Glu |
S236 |
4 | BAA10g13610 | A10 | 14600607 | G | A | missense_variant | MODERATE | c.950C>T|p.Ser317Leu |
S286 |
5 | BAA10g13610 | A10 | 14601555 | G | A | missense_variant | MODERATE | c.434C>T|p.Ser145Phe |
S280 |
6 | BAA10g13610 | A10 | 14601803 | G | A | synonymous_variant | LOW | c.186C>T|p.Val62Val |
S195 |
7 | BAA10g13610 | A10 | 14601942 | G | A | missense_variant | MODERATE | c.47C>T|p.Pro16Leu |
S80 |
8 | BAA10g13610 | A10 | 14603219 | C | T | upstream_gene_variant | MODIFIER | c.-1231G>A| |
S108 |
9 | BAA10g13610 | A10 | 14603929 | C | T | upstream_gene_variant | MODIFIER | c.-1941G>A| |
S271 |
10 | BAA10g13610 | A10 | 14605179 | C | T | upstream_gene_variant | MODIFIER | c.-3191G>A| |
S197 |
11 | BAA10g13610 | A10 | 14605483 | G | A | upstream_gene_variant | MODIFIER | c.-3495C>T| |
S68 |