Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g08970 | A05 | 4492199 | C | T | upstream_gene_variant | MODIFIER | c.-1514C>T| |
S68 |
2 | BAA05g08970 | A05 | 4492356 | G | A | upstream_gene_variant | MODIFIER | c.-1357G>A| |
S298 |
3 | BAA05g08970 | A05 | 4492436 | C | T | upstream_gene_variant | MODIFIER | c.-1277C>T| |
S199 |
4 | BAA05g08970 | A05 | 4493025 | C | T | upstream_gene_variant | MODIFIER | c.-688C>T| |
S270 |
5 | BAA05g08970 | A05 | 4493036 | C | T | upstream_gene_variant | MODIFIER | c.-677C>T| |
S12 |
6 | BAA05g08970 | A05 | 4493693 | C | T | upstream_gene_variant | MODIFIER | c.-20C>T| |
S181 |
7 | BAA05g08970 | A05 | 4493738 | C | T | missense_variant | MODERATE | c.26C>T|p.Ser9Phe |
S14 |
8 | BAA05g08970 | A05 | 4494339 | G | A | synonymous_variant | LOW | c.627G>A|p.Glu209Glu |
S90 |
9 | BAA05g08970 | A05 | 4494406 | C | T | synonymous_variant | LOW | c.694C>T|p.Leu232Leu |
S267 |
10 | BAA05g08970 | A05 | 4494821 | G | A | missense_variant | MODERATE | c.1109G>A|p.Gly370Glu |
S282 |
11 | BAA05g08970 | A05 | 4494858 | G | A | synonymous_variant | LOW | c.1146G>A|p.Glu382Glu |
S179 |
12 | BAA05g08970 | A05 | 4495085 | G | A | missense_variant | MODERATE | c.1373G>A|p.Arg458Lys |
S156 |
13 | BAA05g08970 | A05 | 4497940 | C | T | downstream_gene_variant | MODIFIER | c.*2737C>T| |
S229 |