Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05060 | A10 | 2602307 | G | A | upstream_gene_variant | MODIFIER | c.-4364G>A| |
S161 |
2 | BAA10g05060 | A10 | 2603948 | C | T | upstream_gene_variant | MODIFIER | c.-2723C>T| |
S204 |
3 | BAA10g05060 | A10 | 2604821 | G | A | upstream_gene_variant | MODIFIER | c.-1850G>A| |
S148 S210 S30 S31 |
4 | BAA10g05060 | A10 | 2604933 | G | A | upstream_gene_variant | MODIFIER | c.-1738G>A| |
S237 |
5 | BAA10g05060 | A10 | 2605288 | G | A | upstream_gene_variant | MODIFIER | c.-1383G>A| |
S292 |
6 | BAA10g05060 | A10 | 2605398 | C | T | upstream_gene_variant | MODIFIER | c.-1273C>T| |
S142 S170 |
7 | BAA10g05060 | A10 | 2605527 | G | A | upstream_gene_variant | MODIFIER | c.-1144G>A| |
S292 |
8 | BAA10g05060 | A10 | 2605613 | G | A | upstream_gene_variant | MODIFIER | c.-1058G>A| |
S128 |
9 | BAA10g05060 | A10 | 2605862 | G | A | upstream_gene_variant | MODIFIER | c.-809G>A| |
S57 |
10 | BAA10g05060 | A10 | 2606531 | G | A | upstream_gene_variant | MODIFIER | c.-140G>A| |
S17 |
11 | BAA10g05060 | A10 | 2606762 | C | T | missense_variant | MODERATE | c.92C>T|p.Pro31Leu |
S171 |
12 | BAA10g05060 | A10 | 2607616 | A | C | synonymous_variant | LOW | c.946A>C|p.Arg316Arg |
S302 |
13 | BAA10g05060 | A10 | 2607809 | G | A | missense_variant | MODERATE | c.1139G>A|p.Gly380Glu |
S130 |
14 | BAA10g05060 | A10 | 2607982 | G | A | missense_variant | MODERATE | c.1312G>A|p.Gly438Arg |
S45 |
15 | BAA10g05060 | A10 | 2608979 | G | A | missense_variant | MODERATE | c.2122G>A|p.Glu708Lys |
S211 S227 |