Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g00630 | A10 | 303719 | G | A | downstream_gene_variant | MODIFIER | c.*4184C>T| |
S151 |
2 | BAA10g00630 | A10 | 304013 | C | T | downstream_gene_variant | MODIFIER | c.*3890G>A| |
S165 |
3 | BAA10g00630 | A10 | 308498 | G | A | missense_variant | MODERATE | c.125C>T|p.Ser42Phe |
S179 |
4 | BAA10g00630 | A10 | 308951 | T | A | upstream_gene_variant | MODIFIER | c.-329A>T| |
S63 |
5 | BAA10g00630 | A10 | 309338 | C | T | upstream_gene_variant | MODIFIER | c.-716G>A| |
S110 |
6 | BAA10g00630 | A10 | 309690 | C | T | upstream_gene_variant | MODIFIER | c.-1068G>A| |
S113 |
7 | BAA10g00630 | A10 | 309943 | G | A | upstream_gene_variant | MODIFIER | c.-1321C>T| |
S197 |
8 | BAA10g00630 | A10 | 312282 | G | A | upstream_gene_variant | MODIFIER | c.-3660C>T| |
S172 S217 |
9 | BAA10g00630 | A10 | 312538 | G | A | upstream_gene_variant | MODIFIER | c.-3916C>T| |
S158 |