Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g07380 | A08 | 6137320 | C | T | downstream_gene_variant | MODIFIER | c.*4945G>A| |
S43 |
2 | BAA08g07380 | A08 | 6139115 | G | A | downstream_gene_variant | MODIFIER | c.*3150C>T| |
S115 |
3 | BAA08g07380 | A08 | 6139499 | G | A | downstream_gene_variant | MODIFIER | c.*2766C>T| |
S262 |
4 | BAA08g07380 | A08 | 6140066 | C | T | downstream_gene_variant | MODIFIER | c.*2199G>A| |
S292 |
5 | BAA08g07380 | A08 | 6140162 | G | A | downstream_gene_variant | MODIFIER | c.*2103C>T| |
S202 |
6 | BAA08g07380 | A08 | 6140892 | C | T | downstream_gene_variant | MODIFIER | c.*1373G>A| |
S67 |
7 | BAA08g07380 | A08 | 6141291 | C | T | downstream_gene_variant | MODIFIER | c.*974G>A| |
S113 |
8 | BAA08g07380 | A08 | 6142114 | G | A | downstream_gene_variant | MODIFIER | c.*151C>T| |
S247 |
9 | BAA08g07380 | A08 | 6142659 | G | A | missense_variant | MODERATE | c.47C>T|p.Ala16Val |
S65 |
10 | BAA08g07380 | A08 | 6142810 | T | A | upstream_gene_variant | MODIFIER | c.-105A>T| |
S68 |
11 | BAA08g07380 | A08 | 6144742 | C | T | upstream_gene_variant | MODIFIER | c.-2037G>A| |
S179 |
12 | BAA08g07380 | A08 | 6146289 | G | A | upstream_gene_variant | MODIFIER | c.-3584C>T| |
S125 |
13 | BAA08g07380 | A08 | 6146986 | C | T | upstream_gene_variant | MODIFIER | c.-4281G>A| |
S43 |
14 | BAA08g07380 | A08 | 6147098 | C | T | upstream_gene_variant | MODIFIER | c.-4393G>A| |
S57 |
15 | BAA08g07380 | A08 | 6147319 | G | A | upstream_gene_variant | MODIFIER | c.-4614C>T| |
S124 |