Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g42430 | A05 | 40207682 | C | T | missense_variant | MODERATE | c.3074G>A|p.Gly1025Asp |
S13 |
2 | BAA05g42430 | A05 | 40207720 | G | A | synonymous_variant | LOW | c.3036C>T|p.Pro1012Pro |
S180 |
3 | BAA05g42430 | A05 | 40208098 | C | T | missense_variant | MODERATE | c.2872G>A|p.Val958Met |
S111 |
4 | BAA05g42430 | A05 | 40208916 | C | T | missense_variant&splice_region_variant | MODERATE | c.2389G>A|p.Gly797Arg |
S247 |
5 | BAA05g42430 | A05 | 40209178 | C | T | synonymous_variant | LOW | c.2208G>A|p.Lys736Lys |
S27 |
6 | BAA05g42430 | A05 | 40209422 | C | T | missense_variant | MODERATE | c.2110G>A|p.Val704Ile |
S74 |
7 | BAA05g42430 | A05 | 40210023 | C | T | missense_variant&splice_region_variant | MODERATE | c.1603G>A|p.Glu535Lys |
S210 |
8 | BAA05g42430 | A05 | 40210182 | C | T | missense_variant | MODERATE | c.1519G>A|p.Asp507Asn |
S270 |
9 | BAA05g42430 | A05 | 40211016 | C | T | synonymous_variant | LOW | c.1128G>A|p.Gln376Gln |
S265 |
10 | BAA05g42430 | A05 | 40212114 | C | T | synonymous_variant | LOW | c.246G>A|p.Glu82Glu |
S130 |
11 | BAA05g42430 | A05 | 40215653 | G | A | upstream_gene_variant | MODIFIER | c.-3294C>T| |
S19 |
12 | BAA05g42430 | A05 | 40216978 | C | T | upstream_gene_variant | MODIFIER | c.-4619G>A| |
S270 |