Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g42570 | A05 | 40251081 | C | T | missense_variant | MODERATE | c.544C>T|p.Leu182Phe |
S143 |
2 | BAA05g42570 | A05 | 40251824 | C | T | synonymous_variant | LOW | c.996C>T|p.Ser332Ser |
S117 |
3 | BAA05g42570 | A05 | 40251998 | G | A | missense_variant | MODERATE | c.1039G>A|p.Glu347Lys |
S8 |
4 | BAA05g42570 | A05 | 40252000 | G | A | synonymous_variant | LOW | c.1041G>A|p.Glu347Glu |
S130 |
5 | BAA05g42570 | A05 | 40252013 | C | T | missense_variant | MODERATE | c.1054C>T|p.Leu352Phe |
S282 |
6 | BAA05g42570 | A05 | 40253342 | C | T | intron_variant | MODIFIER | c.1611+88C>T| |
S205 |
7 | BAA05g42570 | A05 | 40253667 | G | A | intron_variant | MODIFIER | c.1716+46G>A| |
S131 |
8 | BAA05g42570 | A05 | 40254102 | C | T | missense_variant | MODERATE | c.1787C>T|p.Ser596Leu |
S62 |
9 | BAA05g42570 | A05 | 40254364 | C | T | intron_variant | MODIFIER | c.1866+18C>T| |
S178 |
10 | BAA05g42570 | A05 | 40255626 | G | A | missense_variant | MODERATE | c.2299G>A|p.Asp767Asn |
S173 |
11 | BAA05g42570 | A05 | 40255920 | G | A | synonymous_variant | LOW | c.2508G>A|p.Glu836Glu |
S53 |
12 | BAA05g42570 | A05 | 40257521 | C | T | synonymous_variant | LOW | c.3396C>T|p.Asp1132Asp |
S39 |
13 | BAA05g42570 | A05 | 40259773 | G | A | downstream_gene_variant | MODIFIER | c.*2174G>A| |
S269 |
14 | BAA05g42570 | A05 | 40260873 | C | T | downstream_gene_variant | MODIFIER | c.*3274C>T| |
S13 |