Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g40340 | A03 | 18853038 | C | T | splice_donor_variant&intron_variant | HIGH | c.2839+1G>A| |
S204 |
2 | BAA03g40340 | A03 | 18853068 | C | T | missense_variant | MODERATE | c.2810G>A|p.Gly937Glu |
S216 |
3 | BAA03g40340 | A03 | 18853164 | G | A | missense_variant | MODERATE | c.2714C>T|p.Thr905Ile |
S262 |
4 | BAA03g40340 | A03 | 18854333 | G | A | splice_region_variant&intron_variant | LOW | c.2039+8C>T| |
S267 |
5 | BAA03g40340 | A03 | 18854439 | C | T | synonymous_variant | LOW | c.1941G>A|p.Leu647Leu |
S281 |
6 | BAA03g40340 | A03 | 18854758 | G | A | missense_variant | MODERATE | c.1699C>T|p.Pro567Ser |
S104 S52 |
7 | BAA03g40340 | A03 | 18855325 | G | A | missense_variant | MODERATE | c.1199C>T|p.Ala400Val |
S128 |
8 | BAA03g40340 | A03 | 18857069 | G | A | missense_variant | MODERATE | c.259C>T|p.Pro87Ser |
S259 |
9 | BAA03g40340 | A03 | 18857148 | C | T | synonymous_variant | LOW | c.180G>A|p.Gly60Gly |
S228 |
10 | BAA03g40340 | A03 | 18857336 | G | A | upstream_gene_variant | MODIFIER | c.-9C>T| |
S30 S31 |
11 | BAA03g40340 | A03 | 18857852 | C | T | upstream_gene_variant | MODIFIER | c.-525G>A| |
S139 |
12 | BAA03g40340 | A03 | 18858136 | G | A | upstream_gene_variant | MODIFIER | c.-809C>T| |
S185 |
13 | BAA03g40340 | A03 | 18858322 | G | A | upstream_gene_variant | MODIFIER | c.-995C>T| |
S126 |
14 | BAA03g40340 | A03 | 18858411 | C | T | upstream_gene_variant | MODIFIER | c.-1084G>A| |
S211 S227 |
15 | BAA03g40340 | A03 | 18858433 | G | A | upstream_gene_variant | MODIFIER | c.-1106C>T| |
S167 |
16 | BAA03g40340 | A03 | 18858527 | G | A | upstream_gene_variant | MODIFIER | c.-1200C>T| |
S169 |
17 | BAA03g40340 | A03 | 18858777 | G | A | upstream_gene_variant | MODIFIER | c.-1450C>T| |
S217 S248 |
18 | BAA03g40340 | A03 | 18858841 | G | A | upstream_gene_variant | MODIFIER | c.-1514C>T| |
S90 |
19 | BAA03g40340 | A03 | 18859078 | G | A | upstream_gene_variant | MODIFIER | c.-1751C>T| |
S138 |