Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g07380 | A03 | 3073402 | G | A | missense_variant | MODERATE | c.4787C>T|p.Ser1596Leu |
S257 |
2 | BAA03g07380 | A03 | 3074543 | C | T | missense_variant | MODERATE | c.3646G>A|p.Ala1216Thr |
S42 |
3 | BAA03g07380 | A03 | 3075736 | G | A | missense_variant | MODERATE | c.2719C>T|p.Leu907Phe |
S178 |
4 | BAA03g07380 | A03 | 3077470 | G | A | missense_variant | MODERATE | c.2131C>T|p.Pro711Ser |
S239 |
5 | BAA03g07380 | A03 | 3078207 | C | T | synonymous_variant | LOW | c.1533G>A|p.Glu511Glu |
S108 |
6 | BAA03g07380 | A03 | 3079690 | C | T | missense_variant&splice_region_variant | MODERATE | c.617G>A|p.Gly206Glu |
S71 |
7 | BAA03g07380 | A03 | 3079764 | G | A | synonymous_variant | LOW | c.543C>T|p.Thr181Thr |
S198 |
8 | BAA03g07380 | A03 | 3080336 | G | A | synonymous_variant | LOW | c.294C>T|p.Phe98Phe |
S174 |
9 | BAA03g07380 | A03 | 3083772 | G | A | upstream_gene_variant | MODIFIER | c.-2491C>T| |
S247 |
10 | BAA03g07380 | A03 | 3083908 | G | A | upstream_gene_variant | MODIFIER | c.-2627C>T| |
S272 |
11 | BAA03g07380 | A03 | 3085764 | G | A | upstream_gene_variant | MODIFIER | c.-4483C>T| |
S47 |
12 | BAA03g07380 | A03 | 3086021 | C | T | upstream_gene_variant | MODIFIER | c.-4740G>A| |
S265 |