Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g09050 | A10 | 11107476 | C | T | upstream_gene_variant | MODIFIER | c.-4277C>T| |
S63 |
2 | BAA10g09050 | A10 | 11107694 | G | A | upstream_gene_variant | MODIFIER | c.-4059G>A| |
S172 |
3 | BAA10g09050 | A10 | 11109916 | G | A | upstream_gene_variant | MODIFIER | c.-1837G>A| |
S295 |
4 | BAA10g09050 | A10 | 11111588 | C | T | upstream_gene_variant | MODIFIER | c.-165C>T| |
S162 |
5 | BAA10g09050 | A10 | 11111640 | G | A | upstream_gene_variant | MODIFIER | c.-113G>A| |
S128 |
6 | BAA10g09050 | A10 | 11112829 | C | T | missense_variant | MODERATE | c.311C>T|p.Ala104Val |
S200 |
7 | BAA10g09050 | A10 | 11112834 | G | A | missense_variant | MODERATE | c.316G>A|p.Ala106Thr |
S1 S90 |
8 | BAA10g09050 | A10 | 11114365 | C | T | intron_variant | MODIFIER | c.804+34C>T| |
S79 S91 |
9 | BAA10g09050 | A10 | 11115966 | G | A | downstream_gene_variant | MODIFIER | c.*1170G>A| |
S125 |
10 | BAA10g09050 | A10 | 11116136 | G | A | downstream_gene_variant | MODIFIER | c.*1340G>A| |
S181 |
11 | BAA10g09050 | A10 | 11117358 | G | A | downstream_gene_variant | MODIFIER | c.*2562G>A| |
S280 |
12 | BAA10g09050 | A10 | 11117404 | G | A | downstream_gene_variant | MODIFIER | c.*2608G>A| |
S57 |
13 | BAA10g09050 | A10 | 11117578 | G | A | downstream_gene_variant | MODIFIER | c.*2782G>A| |
S13 S140 S219 S279 S64 S72 |
14 | BAA10g09050 | A10 | 11117975 | G | A | downstream_gene_variant | MODIFIER | c.*3179G>A| |
S48 |
15 | BAA10g09050 | A10 | 11118544 | C | T | downstream_gene_variant | MODIFIER | c.*3748C>T| |
S20 |
16 | BAA10g09050 | A10 | 11118603 | G | A | downstream_gene_variant | MODIFIER | c.*3807G>A| |
S262 |
17 | BAA10g09050 | A10 | 11119262 | G | A | downstream_gene_variant | MODIFIER | c.*4466G>A| |
S151 S263 |
18 | BAA10g09050 | A10 | 11119543 | C | T | downstream_gene_variant | MODIFIER | c.*4747C>T| |
S156 |