| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 141301 | BAA10g26320 | A10 | 20924333 | C | T | synonymous_variant | LOW | c.2211G>A|p.Gly737Gly |
S256 |
| 141302 | BAA10g26320 | A10 | 20924911 | C | T | missense_variant | MODERATE | c.1633G>A|p.Glu545Lys |
S281 |
| 141303 | BAA10g26320 | A10 | 20925053 | C | T | missense_variant | MODERATE | c.1491G>A|p.Met497Ile |
S165 |
| 141304 | BAA10g26320 | A10 | 20925302 | C | T | synonymous_variant | LOW | c.1242G>A|p.Glu414Glu |
S152 |
| 141305 | BAA10g26320 | A10 | 20927231 | C | T | upstream_gene_variant | MODIFIER | c.-688G>A| |
S272 |
| 141306 | BAA10g26320 | A10 | 20927246 | G | A | upstream_gene_variant | MODIFIER | c.-703C>T| |
S272 |
| 141307 | BAA10g26320 | A10 | 20929278 | C | T | upstream_gene_variant | MODIFIER | c.-2735G>A| |
S236 |
| 141308 | BAA10g26330 | A10 | 20929326 | C | T | missense_variant | MODERATE | c.475G>A|p.Val159Met |
S20 |
| 141309 | BAA10g26330 | A10 | 20929370 | C | T | missense_variant | MODERATE | c.431G>A|p.Gly144Glu |
S195 |
| 141310 | BAA10g26330 | A10 | 20929521 | G | A | missense_variant | MODERATE | c.280C>T|p.Leu94Phe |
S85 |
| 141311 | BAA10g26330 | A10 | 20929564 | C | T | synonymous_variant | LOW | c.237G>A|p.Arg79Arg |
S142 |
| 141312 | BAA10g26320 | A10 | 20929791 | C | T | upstream_gene_variant | MODIFIER | c.-3248G>A| |
S157 S163 |
| 141313 | BAA10g26330 | A10 | 20929843 | G | T | missense_variant | MODERATE | c.181C>A|p.Leu61Met |
S31 |
| 141314 | BAA10g26330 | A10 | 20929982 | C | T | synonymous_variant | LOW | c.42G>A|p.Glu14Glu |
S177 |
| 141315 | BAA10g26340 | A10 | 20931568 | G | A | synonymous_variant | LOW | c.858G>A|p.Glu286Glu |
S270 |
| 141316 | BAA10g26350 | A10 | 20932760 | C | T | missense_variant | MODERATE | c.991G>A|p.Gly331Ser |
S260 |
| 141317 | BAA10g26350 | A10 | 20932783 | C | T | missense_variant | MODERATE | c.968G>A|p.Ser323Asn |
S244 |
| 141318 | BAA10g26350 | A10 | 20933418 | G | A | synonymous_variant | LOW | c.333C>T|p.Leu111Leu |
S1 |
| 141319 | BAA10g26350 | A10 | 20933537 | G | A | missense_variant | MODERATE | c.214C>T|p.Pro72Ser |
S82 S92 |
| 141320 | BAA10g26330 | A10 | 20934055 | G | A | upstream_gene_variant | MODIFIER | c.-4032C>T| |
S77 S82 |
| 141321 | BAA10g26330 | A10 | 20934254 | G | A | upstream_gene_variant | MODIFIER | c.-4231C>T| |
S274 |
| 141322 | BAA10g26350 | A10 | 20935365 | G | A | upstream_gene_variant | MODIFIER | c.-1615C>T| |
S34 |
| 141323 | BAA10g26350 | A10 | 20935611 | G | A | upstream_gene_variant | MODIFIER | c.-1861C>T| |
S32 |
| 141324 | BAA10g26360 | A10 | 20936364 | G | A | missense_variant | MODERATE | c.1042C>T|p.His348Tyr |
S240 |
| 141325 | BAA10g26360 | A10 | 20936869 | C | T | synonymous_variant | LOW | c.537G>A|p.Ser179Ser |
S162 |