Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g34140 | A10 | 24090680 | G | A | upstream_gene_variant | MODIFIER | c.-3208G>A| |
S74 |
2 | BAA10g34140 | A10 | 24091413 | G | A | upstream_gene_variant | MODIFIER | c.-2475G>A| |
S99 |
3 | BAA10g34140 | A10 | 24092123 | G | A | upstream_gene_variant | MODIFIER | c.-1765G>A| |
S263 |
4 | BAA10g34140 | A10 | 24092692 | C | T | upstream_gene_variant | MODIFIER | c.-1196C>T| |
S229 |
5 | BAA10g34140 | A10 | 24092877 | G | A | upstream_gene_variant | MODIFIER | c.-1011G>A| |
S128 |
6 | BAA10g34140 | A10 | 24093354 | C | T | upstream_gene_variant | MODIFIER | c.-534C>T| |
S20 |
7 | BAA10g34140 | A10 | 24093982 | C | T | missense_variant | MODERATE | c.95C>T|p.Ser32Leu |
S246 |
8 | BAA10g34140 | A10 | 24094693 | G | A | missense_variant | MODERATE | c.806G>A|p.Arg269Gln |
S59 |
9 | BAA10g34140 | A10 | 24095235 | C | T | missense_variant | MODERATE | c.1348C>T|p.His450Tyr |
S105 |
10 | BAA10g34140 | A10 | 24095990 | G | A | synonymous_variant | LOW | c.2103G>A|p.Glu701Glu |
S125 |
11 | BAA10g34140 | A10 | 24096025 | G | A | missense_variant | MODERATE | c.2138G>A|p.Cys713Tyr |
S17 |
12 | BAA10g34140 | A10 | 24099567 | G | A | downstream_gene_variant | MODIFIER | c.*3424G>A| |
S132 S137 S138 S215 S89 |
13 | BAA10g34140 | A10 | 24099819 | C | T | downstream_gene_variant | MODIFIER | c.*3676C>T| |
S142 |
14 | BAA10g34140 | A10 | 24099890 | C | A | downstream_gene_variant | MODIFIER | c.*3747C>A| |
S67 |