| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 150501 | BAA10g34470 | A10 | 24231907 | G | A | synonymous_variant | LOW | c.39G>A|p.Pro13Pro |
S299 |
| 150502 | BAA10g34460 | A10 | 24232071 | G | A | upstream_gene_variant | MODIFIER | c.-3661C>T| |
S183 S198 |
| 150503 | BAA10g34470 | A10 | 24232283 | C | T | missense_variant | MODERATE | c.151C>T|p.Pro51Ser |
S20 |
| 150504 | BAA10g34470 | A10 | 24232439 | C | T | missense_variant | MODERATE | c.235C>T|p.Pro79Ser |
S61 |
| 150505 | BAA10g34460 | A10 | 24232532 | C | T | upstream_gene_variant | MODIFIER | c.-4122G>A| |
S47 |
| 150506 | BAA10g34470 | A10 | 24233166 | C | T | missense_variant | MODERATE | c.565C>T|p.Leu189Phe |
S157 S163 |
| 150507 | BAA10g34470 | A10 | 24233517 | G | A | missense_variant | MODERATE | c.847G>A|p.Val283Ile |
S173 |
| 150508 | BAA10g34470 | A10 | 24234613 | G | A | downstream_gene_variant | MODIFIER | c.*374G>A| |
S100 |
| 150509 | BAA10g34470 | A10 | 24235229 | G | A | downstream_gene_variant | MODIFIER | c.*990G>A| |
S35 |
| 150510 | BAA10g34480 | A10 | 24237009 | G | A | missense_variant | MODERATE | c.4540C>T|p.Pro1514Ser |
S50 |
| 150511 | BAA10g34480 | A10 | 24237440 | C | T | missense_variant | MODERATE | c.4187G>A|p.Arg1396Lys |
S234 |
| 150512 | BAA10g34480 | A10 | 24237767 | G | A | stop_gained | HIGH | c.4039C>T|p.Gln1347* |
S209 |
| 150513 | BAA10g34470 | A10 | 24238218 | G | A | downstream_gene_variant | MODIFIER | c.*3979G>A| |
S251 |
| 150514 | BAA10g34480 | A10 | 24238845 | C | T | stop_gained | HIGH | c.3270G>A|p.Trp1090* |
S302 |
| 150515 | BAA10g34480 | A10 | 24239191 | C | T | missense_variant | MODERATE | c.2924G>A|p.Gly975Asp |
S82 S92 |
| 150516 | BAA10g34480 | A10 | 24239251 | G | A | missense_variant | MODERATE | c.2864C>T|p.Thr955Ile |
S303 |
| 150517 | BAA10g34480 | A10 | 24240897 | C | T | missense_variant | MODERATE | c.1669G>A|p.Glu557Lys |
S153 S213 |
| 150518 | BAA10g34480 | A10 | 24241954 | C | T | synonymous_variant | LOW | c.759G>A|p.Glu253Glu |
S168 |
| 150519 | BAA10g34480 | A10 | 24242051 | C | T | missense_variant | MODERATE | c.662G>A|p.Arg221Lys |
S274 |
| 150520 | BAA10g34480 | A10 | 24242149 | G | A | synonymous_variant | LOW | c.564C>T|p.Leu188Leu |
S62 |
| 150521 | BAA10g34480 | A10 | 24242369 | G | A | missense_variant | MODERATE | c.344C>T|p.Ser115Phe |
S228 |
| 150522 | BAA10g34480 | A10 | 24246314 | C | T | upstream_gene_variant | MODIFIER | c.-3536G>A| |
S295 |
| 150523 | BAA10g34480 | A10 | 24246894 | G | A | upstream_gene_variant | MODIFIER | c.-4116C>T| |
S181 |
| 150524 | BAA10g34480 | A10 | 24247144 | G | A | upstream_gene_variant | MODIFIER | c.-4366C>T| |
S250 |
| 150525 | BAA10g34500 | A10 | 24247408 | G | A | synonymous_variant | LOW | c.783G>A|p.Lys261Lys |
S240 |