Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g02220 | A07 | 1699915 | C | T | upstream_gene_variant | MODIFIER | c.-3846C>T| |
S150 |
2 | BAA07g02220 | A07 | 1700426 | C | T | upstream_gene_variant | MODIFIER | c.-3335C>T| |
S191 |
3 | BAA07g02220 | A07 | 1700475 | C | T | upstream_gene_variant | MODIFIER | c.-3286C>T| |
S283 |
4 | BAA07g02220 | A07 | 1701316 | C | T | upstream_gene_variant | MODIFIER | c.-2445C>T| |
S283 |
5 | BAA07g02220 | A07 | 1701831 | C | T | upstream_gene_variant | MODIFIER | c.-1930C>T| |
S247 |
6 | BAA07g02220 | A07 | 1702288 | G | A | upstream_gene_variant | MODIFIER | c.-1473G>A| |
S130 |
7 | BAA07g02220 | A07 | 1702317 | C | T | upstream_gene_variant | MODIFIER | c.-1444C>T| |
S298 |
8 | BAA07g02220 | A07 | 1703324 | G | A | upstream_gene_variant | MODIFIER | c.-437G>A| |
S194 |
9 | BAA07g02220 | A07 | 1705470 | G | A | missense_variant | MODERATE | c.496G>A|p.Ala166Thr |
S262 |
10 | BAA07g02220 | A07 | 1705651 | C | T | synonymous_variant | LOW | c.558C>T|p.Val186Val |
S274 |
11 | BAA07g02220 | A07 | 1706030 | G | A | stop_gained | HIGH | c.815G>A|p.Trp272* |
S245 |
12 | BAA07g02220 | A07 | 1706602 | C | T | downstream_gene_variant | MODIFIER | c.*292C>T| |
S81 S85 |
13 | BAA07g02220 | A07 | 1707443 | C | T | downstream_gene_variant | MODIFIER | c.*1133C>T| |
S230 |