Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g37710 | A03 | 17434701 | C | T | upstream_gene_variant | MODIFIER | c.-4814C>T| |
S191 |
2 | BAA03g37710 | A03 | 17436035 | T | C | upstream_gene_variant | MODIFIER | c.-3480T>C| |
S44 |
3 | BAA03g37710 | A03 | 17436229 | C | T | upstream_gene_variant | MODIFIER | c.-3286C>T| |
S244 |
4 | BAA03g37710 | A03 | 17436508 | G | A | upstream_gene_variant | MODIFIER | c.-3007G>A| |
S283 |
5 | BAA03g37710 | A03 | 17436551 | G | A | upstream_gene_variant | MODIFIER | c.-2964G>A| |
S298 |
6 | BAA03g37710 | A03 | 17439226 | C | T | upstream_gene_variant | MODIFIER | c.-289C>T| |
S96 |
7 | BAA03g37710 | A03 | 17439325 | G | A | upstream_gene_variant | MODIFIER | c.-190G>A| |
S292 |
8 | BAA03g37710 | A03 | 17439675 | C | T | missense_variant | MODERATE | c.161C>T|p.Thr54Ile |
S239 |
9 | BAA03g37710 | A03 | 17440826 | C | T | missense_variant | MODERATE | c.1312C>T|p.His438Tyr |
S40 S49 |
10 | BAA03g37710 | A03 | 17441272 | C | T | synonymous_variant | LOW | c.1758C>T|p.Ile586Ile |
S270 |
11 | BAA03g37710 | A03 | 17441327 | C | T | missense_variant | MODERATE | c.1813C>T|p.Arg605Cys |
S100 |