Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g11760 | A10 | 13336458 | G | A | downstream_gene_variant | MODIFIER | c.*1920C>T| |
S39 |
2 | BAA10g11760 | A10 | 13336783 | C | T | downstream_gene_variant | MODIFIER | c.*1595G>A| |
S168 |
3 | BAA10g11760 | A10 | 13337214 | G | A | downstream_gene_variant | MODIFIER | c.*1164C>T| |
S216 |
4 | BAA10g11760 | A10 | 13337223 | C | T | downstream_gene_variant | MODIFIER | c.*1155G>A| |
S135 S152 S203 |
5 | BAA10g11760 | A10 | 13337385 | C | T | downstream_gene_variant | MODIFIER | c.*993G>A| |
S80 |
6 | BAA10g11760 | A10 | 13337677 | G | A | downstream_gene_variant | MODIFIER | c.*701C>T| |
S28 |
7 | BAA10g11760 | A10 | 13338553 | C | T | missense_variant | MODERATE | c.467G>A|p.Gly156Asp |
S117 |
8 | BAA10g11760 | A10 | 13338717 | G | A | synonymous_variant | LOW | c.303C>T|p.Leu101Leu |
S138 |
9 | BAA10g11760 | A10 | 13338814 | G | A | missense_variant | MODERATE | c.206C>T|p.Ser69Phe |
S112 |
10 | BAA10g11760 | A10 | 13338925 | G | A | missense_variant | MODERATE | c.95C>T|p.Ser32Leu |
S245 |
11 | BAA10g11760 | A10 | 13340172 | C | T | upstream_gene_variant | MODIFIER | c.-1153G>A| |
S166 |
12 | BAA10g11760 | A10 | 13340951 | G | A | upstream_gene_variant | MODIFIER | c.-1932C>T| |
S148 S210 S30 S31 |
13 | BAA10g11760 | A10 | 13343519 | G | A | upstream_gene_variant | MODIFIER | c.-4500C>T| |
S178 |