Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02480 | A02 | 1112095 | G | A | upstream_gene_variant | MODIFIER | c.-4085G>A| |
S136 |
2 | BAA02g02480 | A02 | 1114604 | G | A | upstream_gene_variant | MODIFIER | c.-1576G>A| |
S302 |
3 | BAA02g02480 | A02 | 1115937 | A | T | upstream_gene_variant | MODIFIER | c.-243A>T| |
S252 |
4 | BAA02g02480 | A02 | 1116081 | C | T | upstream_gene_variant | MODIFIER | c.-99C>T| |
S15 S2 S3 S34 |
5 | BAA02g02480 | A02 | 1116163 | G | A | upstream_gene_variant | MODIFIER | c.-17G>A| |
S177 |
6 | BAA02g02480 | A02 | 1116380 | C | T | synonymous_variant | LOW | c.201C>T|p.Phe67Phe |
S264 |
7 | BAA02g02480 | A02 | 1116402 | G | A | missense_variant | MODERATE | c.223G>A|p.Asp75Asn |
S67 |
8 | BAA02g02480 | A02 | 1117087 | C | T | intron_variant | MODIFIER | c.364+544C>T| |
S38 |
9 | BAA02g02480 | A02 | 1118016 | G | A | missense_variant | MODERATE | c.581G>A|p.Arg194Lys |
S5 |
10 | BAA02g02480 | A02 | 1118272 | G | A | synonymous_variant | LOW | c.837G>A|p.Glu279Glu |
S259 |
11 | BAA02g02480 | A02 | 1118868 | G | A | missense_variant | MODERATE | c.1249G>A|p.Glu417Lys |
S293 |
12 | BAA02g02480 | A02 | 1118920 | G | A | missense_variant | MODERATE | c.1301G>A|p.Arg434Lys |
S62 |
13 | BAA02g02480 | A02 | 1119440 | G | A | downstream_gene_variant | MODIFIER | c.*414G>A| |
S163 |
14 | BAA02g02480 | A02 | 1119551 | C | T | downstream_gene_variant | MODIFIER | c.*525C>T| |
S71 |
15 | BAA02g02480 | A02 | 1119743 | C | T | downstream_gene_variant | MODIFIER | c.*717C>T| |
S124 |
16 | BAA02g02480 | A02 | 1120348 | G | A | downstream_gene_variant | MODIFIER | c.*1322G>A| |
S176 |
17 | BAA02g02480 | A02 | 1122058 | C | T | downstream_gene_variant | MODIFIER | c.*3032C>T| |
S118 |