Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05900 | A10 | 3020088 | G | A | upstream_gene_variant | MODIFIER | c.-3571G>A| |
S50 |
2 | BAA10g05900 | A10 | 3020273 | G | A | upstream_gene_variant | MODIFIER | c.-3386G>A| |
S105 S106 |
3 | BAA10g05900 | A10 | 3020358 | G | A | upstream_gene_variant | MODIFIER | c.-3301G>A| |
S160 |
4 | BAA10g05900 | A10 | 3020441 | C | T | upstream_gene_variant | MODIFIER | c.-3218C>T| |
S71 |
5 | BAA10g05900 | A10 | 3020634 | G | A | upstream_gene_variant | MODIFIER | c.-3025G>A| |
S245 |
6 | BAA10g05900 | A10 | 3020650 | A | T | upstream_gene_variant | MODIFIER | c.-3009A>T| |
S208 S93 |
7 | BAA10g05900 | A10 | 3021475 | C | T | upstream_gene_variant | MODIFIER | c.-2184C>T| |
S256 |
8 | BAA10g05900 | A10 | 3021612 | C | T | upstream_gene_variant | MODIFIER | c.-2047C>T| |
S4 |
9 | BAA10g05900 | A10 | 3021837 | C | T | upstream_gene_variant | MODIFIER | c.-1822C>T| |
S210 S225 |
10 | BAA10g05900 | A10 | 3022258 | G | A | upstream_gene_variant | MODIFIER | c.-1401G>A| |
S95 |
11 | BAA10g05900 | A10 | 3022751 | G | A | upstream_gene_variant | MODIFIER | c.-908G>A| |
S211 S227 |
12 | BAA10g05900 | A10 | 3022995 | G | A | upstream_gene_variant | MODIFIER | c.-664G>A| |
S16 |
13 | BAA10g05900 | A10 | 3023967 | G | A | missense_variant | MODERATE | c.82G>A|p.Asp28Asn |
S278 |
14 | BAA10g05900 | A10 | 3024022 | C | T | missense_variant | MODERATE | c.137C>T|p.Ser46Phe |
S260 |
15 | BAA10g05900 | A10 | 3028042 | C | T | downstream_gene_variant | MODIFIER | c.*3737C>T| |
S95 |
16 | BAA10g05900 | A10 | 3028390 | C | T | downstream_gene_variant | MODIFIER | c.*4085C>T| |
S139 |