Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20990 | A01 | 10332215 | C | T | synonymous_variant | LOW | c.2946G>A|p.Thr982Thr |
S295 |
2 | BAA01g20990 | A01 | 10332340 | C | T | missense_variant | MODERATE | c.2821G>A|p.Ala941Thr |
S10 |
3 | BAA01g20990 | A01 | 10332411 | C | T | missense_variant | MODERATE | c.2750G>A|p.Arg917Lys |
S255 |
4 | BAA01g20990 | A01 | 10333027 | C | T | missense_variant | MODERATE | c.2134G>A|p.Ala712Thr |
S65 |
5 | BAA01g20990 | A01 | 10333388 | G | A | stop_gained | HIGH | c.1867C>T|p.Arg623* |
S308 |
6 | BAA01g20990 | A01 | 10333406 | C | T | missense_variant | MODERATE | c.1849G>A|p.Asp617Asn |
S264 |
7 | BAA01g20990 | A01 | 10334396 | G | A | synonymous_variant | LOW | c.931C>T|p.Leu311Leu |
S244 |
8 | BAA01g20990 | A01 | 10334786 | C | T | missense_variant | MODERATE | c.541G>A|p.Glu181Lys |
S61 |
9 | BAA01g20990 | A01 | 10334819 | C | T | missense_variant | MODERATE | c.508G>A|p.Ala170Thr |
S61 |
10 | BAA01g20990 | A01 | 10334826 | C | T | missense_variant | MODERATE | c.501G>A|p.Met167Ile |
S259 |
11 | BAA01g20990 | A01 | 10335830 | C | T | upstream_gene_variant | MODIFIER | c.-504G>A| |
S54 |
12 | BAA01g20990 | A01 | 10336421 | G | A | upstream_gene_variant | MODIFIER | c.-1095C>T| |
S165 |
13 | BAA01g20990 | A01 | 10336701 | G | A | upstream_gene_variant | MODIFIER | c.-1375C>T| |
S180 |
14 | BAA01g20990 | A01 | 10338075 | G | A | upstream_gene_variant | MODIFIER | c.-2749C>T| |
S71 |
15 | BAA01g20990 | A01 | 10339615 | G | A | upstream_gene_variant | MODIFIER | c.-4289C>T| |
S168 |
16 | BAA01g20990 | A01 | 10339630 | C | T | upstream_gene_variant | MODIFIER | c.-4304G>A| |
S250 |
17 | BAA01g20990 | A01 | 10339796 | C | T | upstream_gene_variant | MODIFIER | c.-4470G>A| |
S198 |
18 | BAA01g20990 | A01 | 10340163 | G | A | upstream_gene_variant | MODIFIER | c.-4837C>T| |
S139 |