Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20600 | A10 | 18459291 | C | T | upstream_gene_variant | MODIFIER | c.-4730C>T| |
S238 |
2 | BAA10g20600 | A10 | 18459301 | C | T | upstream_gene_variant | MODIFIER | c.-4720C>T| |
S113 |
3 | BAA10g20600 | A10 | 18460674 | G | A | upstream_gene_variant | MODIFIER | c.-3347G>A| |
S136 |
4 | BAA10g20600 | A10 | 18461046 | C | T | upstream_gene_variant | MODIFIER | c.-2975C>T| |
S185 |
5 | BAA10g20600 | A10 | 18461919 | G | A | upstream_gene_variant | MODIFIER | c.-2102G>A| |
S191 |
6 | BAA10g20600 | A10 | 18462205 | A | T | upstream_gene_variant | MODIFIER | c.-1816A>T| |
S11 S207 S248 S40 S42 S49 S71 |
7 | BAA10g20600 | A10 | 18463297 | T | C | upstream_gene_variant | MODIFIER | c.-724T>C| |
S18 |
8 | BAA10g20600 | A10 | 18463407 | G | A | upstream_gene_variant | MODIFIER | c.-614G>A| |
S125 |
9 | BAA10g20600 | A10 | 18463419 | G | A | upstream_gene_variant | MODIFIER | c.-602G>A| |
S155 |
10 | BAA10g20600 | A10 | 18464701 | G | A | missense_variant&splice_region_variant | MODERATE | c.214G>A|p.Gly72Arg |
S288 |
11 | BAA10g20600 | A10 | 18470114 | C | T | synonymous_variant | LOW | c.1632C>T|p.Thr544Thr |
S260 |