Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16040 | A10 | 16082453 | G | A | upstream_gene_variant | MODIFIER | c.-3143G>A| |
S112 |
2 | BAA10g16040 | A10 | 16082627 | C | T | upstream_gene_variant | MODIFIER | c.-2969C>T| |
S229 |
3 | BAA10g16040 | A10 | 16082911 | C | T | upstream_gene_variant | MODIFIER | c.-2685C>T| |
S194 |
4 | BAA10g16040 | A10 | 16083270 | C | T | upstream_gene_variant | MODIFIER | c.-2326C>T| |
S259 |
5 | BAA10g16040 | A10 | 16085373 | G | A | upstream_gene_variant | MODIFIER | c.-223G>A| |
S4 |
6 | BAA10g16040 | A10 | 16085530 | C | T | upstream_gene_variant | MODIFIER | c.-66C>T| |
S187 |
7 | BAA10g16040 | A10 | 16085630 | C | T | missense_variant | MODERATE | c.35C>T|p.Ser12Phe |
S144 |
8 | BAA10g16040 | A10 | 16086425 | C | T | synonymous_variant | LOW | c.675C>T|p.Tyr225Tyr |
S170 |
9 | BAA10g16040 | A10 | 16086871 | C | T | splice_region_variant&intron_variant | LOW | c.844-8C>T| |
S152 |