Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g34660 | A03 | 16067581 | G | A | synonymous_variant | LOW | c.4821C>T|p.Ile1607Ile |
S186 |
2 | BAA03g34660 | A03 | 16068338 | A | G | missense_variant&splice_region_variant | MODERATE | c.4463T>C|p.Leu1488Ser |
S222 S258 |
3 | BAA03g34660 | A03 | 16068346 | G | A | splice_region_variant&intron_variant | LOW | c.4462-7C>T| |
S161 |
4 | BAA03g34660 | A03 | 16073450 | C | T | intron_variant | MODIFIER | c.2152+102G>A| |
S240 |
5 | BAA03g34660 | A03 | 16073719 | C | T | intron_variant | MODIFIER | c.2071-86G>A| |
S207 |
6 | BAA03g34660 | A03 | 16073809 | C | T | intron_variant | MODIFIER | c.2070+39G>A| |
S153 |
7 | BAA03g34660 | A03 | 16076410 | C | T | missense_variant | MODERATE | c.796G>A|p.Asp266Asn |
S90 |
8 | BAA03g34660 | A03 | 16077238 | G | A | missense_variant | MODERATE | c.548C>T|p.Pro183Leu |
S261 |
9 | BAA03g34660 | A03 | 16077298 | C | T | missense_variant | MODERATE | c.488G>A|p.Arg163Lys |
S70 |
10 | BAA03g34660 | A03 | 16077808 | G | A | missense_variant | MODERATE | c.224C>T|p.Ser75Leu |
S135 |
11 | BAA03g34660 | A03 | 16078087 | C | T | stop_gained | HIGH | c.24G>A|p.Trp8* |
S121 |
12 | BAA03g34660 | A03 | 16079613 | G | A | upstream_gene_variant | MODIFIER | c.-1503C>T| |
S197 |
13 | BAA03g34660 | A03 | 16079646 | C | T | upstream_gene_variant | MODIFIER | c.-1536G>A| |
S281 |
14 | BAA03g34660 | A03 | 16080272 | G | A | upstream_gene_variant | MODIFIER | c.-2162C>T| |
S69 |
15 | BAA03g34660 | A03 | 16080379 | G | A | upstream_gene_variant | MODIFIER | c.-2269C>T| |
S89 |
16 | BAA03g34660 | A03 | 16080878 | C | T | upstream_gene_variant | MODIFIER | c.-2768G>A| |
S40 S49 |
17 | BAA03g34660 | A03 | 16083003 | G | A | upstream_gene_variant | MODIFIER | c.-4893C>T| |
S59 |