Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g61770 | A03 | 31259229 | G | A | downstream_gene_variant | MODIFIER | c.*4148C>T| |
S191 |
2 | BAA03g61770 | A03 | 31260111 | G | A | downstream_gene_variant | MODIFIER | c.*3266C>T| |
S132 S137 S215 S89 |
3 | BAA03g61770 | A03 | 31261997 | C | T | downstream_gene_variant | MODIFIER | c.*1380G>A| |
S47 |
4 | BAA03g61770 | A03 | 31263207 | C | T | downstream_gene_variant | MODIFIER | c.*170G>A| |
S131 |
5 | BAA03g61770 | A03 | 31263411 | G | A | missense_variant | MODERATE | c.2327C>T|p.Ala776Val |
S260 |
6 | BAA03g61770 | A03 | 31263576 | G | A | missense_variant | MODERATE | c.2162C>T|p.Ser721Phe |
S250 |
7 | BAA03g61770 | A03 | 31263787 | C | T | missense_variant | MODERATE | c.1951G>A|p.Val651Met |
S35 |
8 | BAA03g61770 | A03 | 31265683 | C | T | missense_variant | MODERATE | c.316G>A|p.Ala106Thr |
S81 S85 |
9 | BAA03g61770 | A03 | 31265992 | C | T | missense_variant | MODERATE | c.7G>A|p.Gly3Ser |
S293 |
10 | BAA03g61770 | A03 | 31266067 | G | A | upstream_gene_variant | MODIFIER | c.-69C>T| |
S262 |
11 | BAA03g61770 | A03 | 31267233 | G | A | upstream_gene_variant | MODIFIER | c.-1235C>T| |
S171 |
12 | BAA03g61770 | A03 | 31267707 | G | A | upstream_gene_variant | MODIFIER | c.-1709C>T| |
S128 |
13 | BAA03g61770 | A03 | 31267853 | C | T | upstream_gene_variant | MODIFIER | c.-1855G>A| |
S208 S93 |
14 | BAA03g61770 | A03 | 31268770 | G | A | upstream_gene_variant | MODIFIER | c.-2772C>T| |
S223 |
15 | BAA03g61770 | A03 | 31268945 | C | T | upstream_gene_variant | MODIFIER | c.-2947G>A| |
S89 |
16 | BAA03g61770 | A03 | 31269371 | G | A | upstream_gene_variant | MODIFIER | c.-3373C>T| |
S257 |
17 | BAA03g61770 | A03 | 31269375 | C | T | upstream_gene_variant | MODIFIER | c.-3377G>A| |
S202 |