Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g12260 | A10 | 13706866 | C | T | upstream_gene_variant | MODIFIER | c.-4766C>T| |
S164 |
2 | BAA10g12260 | A10 | 13707115 | G | A | upstream_gene_variant | MODIFIER | c.-4517G>A| |
S1 S90 |
3 | BAA10g12260 | A10 | 13710002 | G | A | upstream_gene_variant | MODIFIER | c.-1630G>A| |
S155 S211 |
4 | BAA10g12260 | A10 | 13710422 | G | A | upstream_gene_variant | MODIFIER | c.-1210G>A| |
S88 |
5 | BAA10g12260 | A10 | 13710626 | C | T | upstream_gene_variant | MODIFIER | c.-1006C>T| |
S46 |
6 | BAA10g12260 | A10 | 13710715 | G | A | upstream_gene_variant | MODIFIER | c.-917G>A| |
S192 |
7 | BAA10g12260 | A10 | 13710887 | G | A | upstream_gene_variant | MODIFIER | c.-745G>A| |
S264 |
8 | BAA10g12260 | A10 | 13711299 | G | A | upstream_gene_variant | MODIFIER | c.-333G>A| |
S296 |
9 | BAA10g12260 | A10 | 13711568 | C | T | upstream_gene_variant | MODIFIER | c.-64C>T| |
S11 |
10 | BAA10g12260 | A10 | 13712618 | G | A | missense_variant | MODERATE | c.767G>A|p.Gly256Glu |
S262 |
11 | BAA10g12260 | A10 | 13713912 | G | A | downstream_gene_variant | MODIFIER | c.*1257G>A| |
S241 |
12 | BAA10g12260 | A10 | 13714300 | C | T | downstream_gene_variant | MODIFIER | c.*1645C>T| |
S104 S52 |
13 | BAA10g12260 | A10 | 13714380 | G | A | downstream_gene_variant | MODIFIER | c.*1725G>A| |
S261 |