Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g05660 | A07 | 5731961 | C | T | upstream_gene_variant | MODIFIER | c.-4379C>T| |
S163 |
2 | BAA07g05660 | A07 | 5732501 | G | A | upstream_gene_variant | MODIFIER | c.-3839G>A| |
S217 |
3 | BAA07g05660 | A07 | 5733169 | G | A | upstream_gene_variant | MODIFIER | c.-3171G>A| |
S36 |
4 | BAA07g05660 | A07 | 5733232 | C | T | upstream_gene_variant | MODIFIER | c.-3108C>T| |
S268 |
5 | BAA07g05660 | A07 | 5733646 | G | A | upstream_gene_variant | MODIFIER | c.-2694G>A| |
S213 |
6 | BAA07g05660 | A07 | 5734090 | G | A | upstream_gene_variant | MODIFIER | c.-2250G>A| |
S195 |
7 | BAA07g05660 | A07 | 5734169 | G | A | upstream_gene_variant | MODIFIER | c.-2171G>A| |
S270 |
8 | BAA07g05660 | A07 | 5734217 | G | A | upstream_gene_variant | MODIFIER | c.-2123G>A| |
S230 |
9 | BAA07g05660 | A07 | 5734561 | C | T | upstream_gene_variant | MODIFIER | c.-1779C>T| |
S206 S26 |
10 | BAA07g05660 | A07 | 5734672 | C | T | upstream_gene_variant | MODIFIER | c.-1668C>T| |
S202 |
11 | BAA07g05660 | A07 | 5736494 | G | A | stop_gained | HIGH | c.155G>A|p.Trp52* |
S231 |
12 | BAA07g05660 | A07 | 5736726 | G | A | stop_gained | HIGH | c.387G>A|p.Trp129* |
S294 |
13 | BAA07g05660 | A07 | 5737273 | C | T | missense_variant | MODERATE | c.934C>T|p.Arg312Trp |
S235 |
14 | BAA07g05660 | A07 | 5738142 | C | T | downstream_gene_variant | MODIFIER | c.*663C>T| |
S193 |
15 | BAA07g05660 | A07 | 5738650 | C | T | downstream_gene_variant | MODIFIER | c.*1171C>T| |
S234 |
16 | BAA07g05660 | A07 | 5739617 | G | A | downstream_gene_variant | MODIFIER | c.*2138G>A| |
S168 |