Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g08950 | A10 | 10990345 | C | T | downstream_gene_variant | MODIFIER | c.*4664G>A| |
S114 |
2 | BAA10g08950 | A10 | 10991312 | C | T | downstream_gene_variant | MODIFIER | c.*3697G>A| |
S281 |
3 | BAA10g08950 | A10 | 10991605 | G | A | downstream_gene_variant | MODIFIER | c.*3404C>T| |
S55 |
4 | BAA10g08950 | A10 | 10992117 | T | C | downstream_gene_variant | MODIFIER | c.*2892A>G| |
S240 |
5 | BAA10g08950 | A10 | 10992237 | G | A | downstream_gene_variant | MODIFIER | c.*2772C>T| |
S129 |
6 | BAA10g08950 | A10 | 10992254 | C | T | downstream_gene_variant | MODIFIER | c.*2755G>A| |
S144 S189 |
7 | BAA10g08950 | A10 | 10992306 | G | A | downstream_gene_variant | MODIFIER | c.*2703C>T| |
S245 |
8 | BAA10g08950 | A10 | 10995626 | G | A | intron_variant | MODIFIER | c.579+92C>T| |
S251 |
9 | BAA10g08950 | A10 | 10996688 | C | T | intron_variant | MODIFIER | c.47-31G>A| |
S157 |
10 | BAA10g08950 | A10 | 10996807 | C | T | stop_gained | HIGH | c.24G>A|p.Trp8* |
S42 |
11 | BAA10g08950 | A10 | 10998491 | C | T | upstream_gene_variant | MODIFIER | c.-1661G>A| |
S173 |
12 | BAA10g08950 | A10 | 10999897 | G | A | upstream_gene_variant | MODIFIER | c.-3067C>T| |
S15 S3 |
13 | BAA10g08950 | A10 | 11000814 | C | T | upstream_gene_variant | MODIFIER | c.-3984G>A| |
S270 |
14 | BAA10g08950 | A10 | 11000991 | C | T | upstream_gene_variant | MODIFIER | c.-4161G>A| |
S142 |
15 | BAA10g08950 | A10 | 11001640 | G | A | upstream_gene_variant | MODIFIER | c.-4810C>T| |
S283 |