Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g41360 | A03 | 19379961 | C | T | missense_variant | MODERATE | c.2273G>A|p.Gly758Asp |
S207 |
2 | BAA03g41360 | A03 | 19381190 | C | T | synonymous_variant | LOW | c.1458G>A|p.Lys486Lys |
S136 |
3 | BAA03g41360 | A03 | 19381210 | G | A | missense_variant | MODERATE | c.1438C>T|p.Pro480Ser |
S168 |
4 | BAA03g41360 | A03 | 19381555 | C | T | missense_variant | MODERATE | c.1285G>A|p.Gly429Arg |
S121 |
5 | BAA03g41360 | A03 | 19382001 | G | A | synonymous_variant | LOW | c.1008C>T|p.Ile336Ile |
S149 |
6 | BAA03g41360 | A03 | 19382377 | C | T | splice_region_variant&intron_variant | LOW | c.636-4G>A| |
S294 |
7 | BAA03g41360 | A03 | 19382738 | G | A | intron_variant | MODIFIER | c.635+238C>T| |
S203 |
8 | BAA03g41360 | A03 | 19383039 | G | A | missense_variant | MODERATE | c.572C>T|p.Thr191Ile |
S56 |
9 | BAA03g41360 | A03 | 19383405 | G | A | missense_variant | MODERATE | c.206C>T|p.Thr69Ile |
S197 |
10 | BAA03g41360 | A03 | 19383685 | G | A | missense_variant | MODERATE | c.14C>T|p.Pro5Leu |
S277 |
11 | BAA03g41360 | A03 | 19384025 | C | T | upstream_gene_variant | MODIFIER | c.-327G>A| |
S250 |
12 | BAA03g41360 | A03 | 19384461 | C | T | upstream_gene_variant | MODIFIER | c.-763G>A| |
S36 |
13 | BAA03g41360 | A03 | 19384752 | C | T | upstream_gene_variant | MODIFIER | c.-1054G>A| |
S182 |
14 | BAA03g41360 | A03 | 19385453 | C | T | upstream_gene_variant | MODIFIER | c.-1755G>A| |
S204 |
15 | BAA03g41360 | A03 | 19385964 | G | A | upstream_gene_variant | MODIFIER | c.-2266C>T| |
S260 |
16 | BAA03g41360 | A03 | 19386814 | G | A | upstream_gene_variant | MODIFIER | c.-3116C>T| |
S168 |
17 | BAA03g41360 | A03 | 19388572 | G | A | upstream_gene_variant | MODIFIER | c.-4874C>T| |
S164 |