Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00060 | A08 | 57379 | G | A | downstream_gene_variant | MODIFIER | c.*4469C>T| |
S308 |
2 | BAA08g00060 | A08 | 57820 | A | C | downstream_gene_variant | MODIFIER | c.*4028T>G| |
S119 |
3 | BAA08g00060 | A08 | 57928 | G | A | downstream_gene_variant | MODIFIER | c.*3920C>T| |
S130 |
4 | BAA08g00060 | A08 | 58361 | G | A | downstream_gene_variant | MODIFIER | c.*3487C>T| |
S202 |
5 | BAA08g00060 | A08 | 58843 | C | T | downstream_gene_variant | MODIFIER | c.*3005G>A| |
S104 S52 |
6 | BAA08g00060 | A08 | 59118 | G | A | downstream_gene_variant | MODIFIER | c.*2730C>T| |
S108 |
7 | BAA08g00060 | A08 | 59145 | G | A | downstream_gene_variant | MODIFIER | c.*2703C>T| |
S1 S90 |
8 | BAA08g00060 | A08 | 60762 | C | T | downstream_gene_variant | MODIFIER | c.*1086G>A| |
S275 |
9 | BAA08g00060 | A08 | 61081 | C | T | downstream_gene_variant | MODIFIER | c.*767G>A| |
S140 |
10 | BAA08g00060 | A08 | 62913 | C | T | missense_variant | MODERATE | c.16G>A|p.Ala6Thr |
S46 |
11 | BAA08g00060 | A08 | 62997 | C | T | upstream_gene_variant | MODIFIER | c.-69G>A| |
S67 |
12 | BAA08g00060 | A08 | 63452 | G | A | upstream_gene_variant | MODIFIER | c.-524C>T| |
S68 |
13 | BAA08g00060 | A08 | 63481 | C | T | upstream_gene_variant | MODIFIER | c.-553G>A| |
S43 |
14 | BAA08g00060 | A08 | 63743 | C | T | upstream_gene_variant | MODIFIER | c.-815G>A| |
S215 |
15 | BAA08g00060 | A08 | 67403 | G | A | upstream_gene_variant | MODIFIER | c.-4475C>T| |
S297 |