Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g00700 | A07 | 435068 | C | T | upstream_gene_variant | MODIFIER | c.-4790C>T| |
S32 |
2 | BAA07g00700 | A07 | 435107 | G | A | upstream_gene_variant | MODIFIER | c.-4751G>A| |
S193 |
3 | BAA07g00700 | A07 | 435195 | C | T | upstream_gene_variant | MODIFIER | c.-4663C>T| |
S138 |
4 | BAA07g00700 | A07 | 435326 | C | T | upstream_gene_variant | MODIFIER | c.-4532C>T| |
S45 |
5 | BAA07g00700 | A07 | 435534 | G | A | upstream_gene_variant | MODIFIER | c.-4324G>A| |
S268 |
6 | BAA07g00700 | A07 | 435556 | G | A | upstream_gene_variant | MODIFIER | c.-4302G>A| |
S65 |
7 | BAA07g00700 | A07 | 437084 | C | T | upstream_gene_variant | MODIFIER | c.-2774C>T| |
S277 |
8 | BAA07g00700 | A07 | 438677 | C | T | upstream_gene_variant | MODIFIER | c.-1181C>T| |
S42 |
9 | BAA07g00700 | A07 | 438744 | C | T | upstream_gene_variant | MODIFIER | c.-1114C>T| |
S197 |
10 | BAA07g00700 | A07 | 440401 | G | A | synonymous_variant | LOW | c.465G>A|p.Arg155Arg |
S278 |
11 | BAA07g00700 | A07 | 441280 | C | T | splice_region_variant&intron_variant | LOW | c.1011+8C>T| |
S128 |
12 | BAA07g00700 | A07 | 441745 | C | T | missense_variant | MODERATE | c.1228C>T|p.Pro410Ser |
S297 |
13 | BAA07g00700 | A07 | 442387 | G | A | downstream_gene_variant | MODIFIER | c.*353G>A| |
S263 |
14 | BAA07g00700 | A07 | 442409 | C | T | downstream_gene_variant | MODIFIER | c.*375C>T| |
S142 |
15 | BAA07g00700 | A07 | 442478 | G | A | downstream_gene_variant | MODIFIER | c.*444G>A| |
S235 |