| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 124251 | BAA10g13920 | A10 | 14802753 | G | A | missense_variant | MODERATE | c.904G>A|p.Gly302Arg |
S77 S82 |
| 124252 | BAA10g13930 | A10 | 14804090 | C | T | upstream_gene_variant | MODIFIER | c.-2361C>T| |
S163 |
| 124253 | BAA10g13930 | A10 | 14806204 | C | T | upstream_gene_variant | MODIFIER | c.-247C>T| |
S23 |
| 124254 | BAA10g13930 | A10 | 14806482 | C | T | missense_variant | MODERATE | c.32C>T|p.Pro11Leu |
S173 S176 |
| 124255 | BAA10g13930 | A10 | 14806607 | G | A | missense_variant | MODERATE | c.157G>A|p.Glu53Lys |
S198 |
| 124256 | BAA10g13960 | A10 | 14808624 | C | T | upstream_gene_variant | MODIFIER | c.-4737C>T| |
S301 S304 |
| 124257 | BAA10g13960 | A10 | 14808988 | G | A | upstream_gene_variant | MODIFIER | c.-4373G>A| |
S1 S90 |
| 124258 | BAA10g13940 | A10 | 14811480 | G | A | upstream_gene_variant | MODIFIER | c.-1023C>T| |
S192 |
| 124259 | BAA10g13940 | A10 | 14812079 | G | A | upstream_gene_variant | MODIFIER | c.-1622C>T| |
S230 |
| 124260 | BAA10g13960 | A10 | 14813703 | G | A | missense_variant | MODERATE | c.343G>A|p.Asp115Asn |
S74 |
| 124261 | BAA10g13960 | A10 | 14813761 | C | T | missense_variant | MODERATE | c.401C>T|p.Ser134Phe |
S256 |
| 124262 | BAA10g13960 | A10 | 14814510 | G | A | missense_variant | MODERATE | c.1150G>A|p.Asp384Asn |
S155 |
| 124263 | BAA10g13960 | A10 | 14815439 | G | A | synonymous_variant | LOW | c.2079G>A|p.Leu693Leu |
S279 |
| 124264 | BAA10g13960 | A10 | 14815604 | C | T | synonymous_variant | LOW | c.2244C>T|p.Arg748Arg |
S115 |
| 124265 | BAA10g13960 | A10 | 14815928 | C | T | synonymous_variant | LOW | c.2568C>T|p.Thr856Thr |
S252 |
| 124266 | BAA10g13970 | A10 | 14817716 | G | A | missense_variant | MODERATE | c.233C>T|p.Thr78Ile |
S66 |
| 124267 | BAA10g13970 | A10 | 14817745 | G | A | synonymous_variant | LOW | c.204C>T|p.Phe68Phe |
S67 |
| 124268 | BAA10g13970 | A10 | 14817894 | C | T | missense_variant | MODERATE | c.55G>A|p.Gly19Ser |
S244 |
| 124269 | BAA10g13950 | A10 | 14817952 | G | A | upstream_gene_variant | MODIFIER | c.-4797C>T| |
S129 |
| 124270 | BAA10g13970 | A10 | 14819650 | G | A | upstream_gene_variant | MODIFIER | c.-1702C>T| |
S159 S243 |
| 124271 | BAA10g13970 | A10 | 14819901 | G | T | upstream_gene_variant | MODIFIER | c.-1953C>A| |
S25 |
| 124272 | BAA10g13970 | A10 | 14819981 | C | T | upstream_gene_variant | MODIFIER | c.-2033G>A| |
S297 |
| 124273 | BAA10g13970 | A10 | 14820191 | G | A | upstream_gene_variant | MODIFIER | c.-2243C>T| |
S172 S217 |
| 124274 | BAA10g13970 | A10 | 14820876 | G | A | upstream_gene_variant | MODIFIER | c.-2928C>T| |
S295 |
| 124275 | BAA10g13970 | A10 | 14821358 | G | A | upstream_gene_variant | MODIFIER | c.-3410C>T| |
S148 S30 S31 S93 |