Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g37020 | A09 | 45190177 | C | T | upstream_gene_variant | MODIFIER | c.-3181C>T| |
S246 |
2 | BAA09g37020 | A09 | 45191028 | G | A | upstream_gene_variant | MODIFIER | c.-2330G>A| |
S10 |
3 | BAA09g37020 | A09 | 45191436 | G | A | upstream_gene_variant | MODIFIER | c.-1922G>A| |
S301 |
4 | BAA09g37020 | A09 | 45191849 | C | T | upstream_gene_variant | MODIFIER | c.-1509C>T| |
S155 S211 |
5 | BAA09g37020 | A09 | 45191933 | C | T | upstream_gene_variant | MODIFIER | c.-1425C>T| |
S76 |
6 | BAA09g37020 | A09 | 45192013 | G | A | upstream_gene_variant | MODIFIER | c.-1345G>A| |
S167 |
7 | BAA09g37020 | A09 | 45192538 | G | A | upstream_gene_variant | MODIFIER | c.-820G>A| |
S172 S217 |
8 | BAA09g37020 | A09 | 45193915 | G | A | stop_gained | HIGH | c.467G>A|p.Trp156* |
S226 |
9 | BAA09g37020 | A09 | 45193980 | C | T | synonymous_variant | LOW | c.532C>T|p.Leu178Leu |
S212 |
10 | BAA09g37020 | A09 | 45194340 | G | A | missense_variant | MODERATE | c.892G>A|p.Gly298Arg |
S200 |
11 | BAA09g37020 | A09 | 45198626 | C | T | downstream_gene_variant | MODIFIER | c.*4134C>T| |
S241 |