Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g26720 | A08 | 19018076 | C | T | synonymous_variant | LOW | c.1494G>A|p.Gly498Gly |
S124 |
2 | BAA08g26720 | A08 | 19018699 | C | T | missense_variant | MODERATE | c.964G>A|p.Asp322Asn |
S132 S137 S89 |
3 | BAA08g26720 | A08 | 19019154 | C | T | missense_variant | MODERATE | c.509G>A|p.Gly170Glu |
S57 |
4 | BAA08g26720 | A08 | 19019239 | G | A | missense_variant | MODERATE | c.424C>T|p.His142Tyr |
S87 |
5 | BAA08g26720 | A08 | 19019266 | C | T | missense_variant | MODERATE | c.397G>A|p.Ala133Thr |
S247 |
6 | BAA08g26720 | A08 | 19019338 | G | A | missense_variant | MODERATE | c.325C>T|p.His109Tyr |
S107 |
7 | BAA08g26720 | A08 | 19019770 | G | A | upstream_gene_variant | MODIFIER | c.-108C>T| |
S117 |
8 | BAA08g26720 | A08 | 19022363 | C | T | upstream_gene_variant | MODIFIER | c.-2701G>A| |
S112 |
9 | BAA08g26720 | A08 | 19024070 | C | T | upstream_gene_variant | MODIFIER | c.-4408G>A| |
S120 |
10 | BAA08g26720 | A08 | 19024075 | C | T | upstream_gene_variant | MODIFIER | c.-4413G>A| |
S54 |
11 | BAA08g26720 | A08 | 19024636 | G | A | upstream_gene_variant | MODIFIER | c.-4974C>T| |
S287 |