Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12980 | A10 | 14244781 | G | A | upstream_gene_variant | MODIFIER | c.-4327G>A| |
S68 |
2 | BAA10g12980 | A10 | 14245098 | C | T | upstream_gene_variant | MODIFIER | c.-4010C>T| |
S44 |
3 | BAA10g12980 | A10 | 14246315 | C | T | upstream_gene_variant | MODIFIER | c.-2793C>T| |
S232 |
4 | BAA10g12980 | A10 | 14247431 | G | A | upstream_gene_variant | MODIFIER | c.-1677G>A| |
S255 |
5 | BAA10g12980 | A10 | 14247951 | G | A | upstream_gene_variant | MODIFIER | c.-1157G>A| |
S261 |
6 | BAA10g12980 | A10 | 14248789 | G | A | upstream_gene_variant | MODIFIER | c.-319G>A| |
S291 |
7 | BAA10g12980 | A10 | 14248835 | C | T | upstream_gene_variant | MODIFIER | c.-273C>T| |
S133 |
8 | BAA10g12980 | A10 | 14249940 | G | A | synonymous_variant | LOW | c.315G>A|p.Glu105Glu |
S264 |
9 | BAA10g12980 | A10 | 14250037 | C | T | missense_variant | MODERATE | c.412C>T|p.Leu138Phe |
S170 |
10 | BAA10g12980 | A10 | 14250830 | G | A | downstream_gene_variant | MODIFIER | c.*24G>A| |
S217 S248 |