| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 46251 | BAA01g27460 | A01 | 15854571 | C | T | missense_variant | MODERATE | c.785G>A|p.Arg262Lys |
S179 |
| 46252 | BAA01g27460 | A01 | 15854791 | C | T | missense_variant | MODERATE | c.565G>A|p.Glu189Lys |
S171 |
| 46253 | BAA01g27450 | A01 | 15855667 | C | T | upstream_gene_variant | MODIFIER | c.-4323G>A| |
S264 |
| 46254 | BAA01g27450 | A01 | 15856287 | G | A | upstream_gene_variant | MODIFIER | c.-4943C>T| |
S228 |
| 46255 | BAA01g27460 | A01 | 15856659 | G | A | upstream_gene_variant | MODIFIER | c.-1304C>T| |
S86 |
| 46256 | BAA01g27460 | A01 | 15856978 | G | A | upstream_gene_variant | MODIFIER | c.-1623C>T| |
S172 S217 |
| 46257 | BAA01g27460 | A01 | 15856986 | C | T | upstream_gene_variant | MODIFIER | c.-1631G>A| |
S4 |
| 46258 | BAA01g27470 | A01 | 15857733 | C | T | missense_variant | MODERATE | c.3890G>A|p.Arg1297Lys |
S267 |
| 46259 | BAA01g27470 | A01 | 15858207 | C | T | synonymous_variant | LOW | c.3510G>A|p.Gln1170Gln |
S146 |
| 46260 | BAA01g27460 | A01 | 15858555 | C | T | upstream_gene_variant | MODIFIER | c.-3200G>A| |
S171 |
| 46261 | BAA01g27460 | A01 | 15858686 | G | A | upstream_gene_variant | MODIFIER | c.-3331C>T| |
S124 |
| 46262 | BAA01g27470 | A01 | 15860361 | G | A | synonymous_variant | LOW | c.2118C>T|p.Cys706Cys |
S240 |
| 46263 | BAA01g27470 | A01 | 15860483 | C | T | missense_variant | MODERATE | c.1996G>A|p.Ala666Thr |
S204 |
| 46264 | BAA01g27470 | A01 | 15861165 | C | T | intron_variant | MODIFIER | c.1469+58G>A| |
S189 |
| 46265 | BAA01g27470 | A01 | 15861568 | G | A | missense_variant | MODERATE | c.1124C>T|p.Ala375Val |
S174 |
| 46266 | BAA01g27470 | A01 | 15861570 | C | T | synonymous_variant | LOW | c.1122G>A|p.Gly374Gly |
S125 |
| 46267 | BAA01g27470 | A01 | 15861762 | C | T | synonymous_variant | LOW | c.930G>A|p.Gly310Gly |
S35 |
| 46268 | BAA01g27470 | A01 | 15861920 | C | T | intron_variant | MODIFIER | c.783-11G>A| |
S276 |
| 46269 | BAA01g27470 | A01 | 15862069 | G | A | intron_variant | MODIFIER | c.783-160C>T| |
S6 |
| 46270 | BAA01g27470 | A01 | 15862678 | C | T | missense_variant | MODERATE | c.427G>A|p.Glu143Lys |
S28 |
| 46271 | BAA01g27470 | A01 | 15862770 | C | T | missense_variant | MODERATE | c.335G>A|p.Ser112Asn |
S80 |
| 46272 | BAA01g27470 | A01 | 15862858 | C | T | missense_variant | MODERATE | c.247G>A|p.Asp83Asn |
S38 |
| 46273 | BAA01g27470 | A01 | 15863126 | C | T | upstream_gene_variant | MODIFIER | c.-22G>A| |
S135 |
| 46274 | BAA01g27470 | A01 | 15864904 | C | T | upstream_gene_variant | MODIFIER | c.-1800G>A| |
S186 |
| 46275 | BAA01g27470 | A01 | 15865992 | C | T | upstream_gene_variant | MODIFIER | c.-2888G>A| |
S108 |