| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 132301 | BAA10g19270 | A10 | 17723354 | G | A | synonymous_variant | LOW | c.819C>T|p.Arg273Arg |
S151 S263 |
| 132302 | BAA10g19270 | A10 | 17723431 | C | T | missense_variant | MODERATE | c.742G>A|p.Asp248Asn |
S209 |
| 132303 | BAA10g19280 | A10 | 17726988 | G | A | missense_variant | MODERATE | c.31G>A|p.Gly11Arg |
S53 |
| 132304 | BAA10g19280 | A10 | 17726989 | G | A | missense_variant | MODERATE | c.32G>A|p.Gly11Glu |
S237 |
| 132305 | BAA10g19280 | A10 | 17727320 | G | A | synonymous_variant | LOW | c.363G>A|p.Gly121Gly |
S192 |
| 132306 | BAA10g19270 | A10 | 17728433 | C | T | upstream_gene_variant | MODIFIER | c.-1966G>A| |
S12 |
| 132307 | BAA10g19270 | A10 | 17729594 | C | T | upstream_gene_variant | MODIFIER | c.-3127G>A| |
S25 |
| 132308 | BAA10g19270 | A10 | 17730061 | C | T | upstream_gene_variant | MODIFIER | c.-3594G>A| |
S229 |
| 132309 | BAA10g19270 | A10 | 17730471 | C | T | upstream_gene_variant | MODIFIER | c.-4004G>A| |
S211 S227 |
| 132310 | BAA10g19270 | A10 | 17731175 | G | A | upstream_gene_variant | MODIFIER | c.-4708C>T| |
S53 |
| 132311 | BAA10g19290 | A10 | 17732889 | C | T | downstream_gene_variant | MODIFIER | c.*3638C>T| |
S11 |
| 132312 | BAA10g19290 | A10 | 17733505 | G | T | downstream_gene_variant | MODIFIER | c.*4254G>T| |
S298 |
| 132313 | BAA10g19290 | A10 | 17733621 | G | A | downstream_gene_variant | MODIFIER | c.*4370G>A| |
S179 |
| 132314 | BAA10g19300 | A10 | 17734923 | C | T | downstream_gene_variant | MODIFIER | c.*1385G>A| |
S188 |
| 132315 | BAA10g19300 | A10 | 17735377 | G | A | downstream_gene_variant | MODIFIER | c.*931C>T| |
S42 |
| 132316 | BAA10g19300 | A10 | 17735632 | G | A | downstream_gene_variant | MODIFIER | c.*676C>T| |
S74 |
| 132317 | BAA10g19300 | A10 | 17736564 | G | A | missense_variant | MODERATE | c.962C>T|p.Ser321Phe |
S165 |
| 132318 | BAA10g19300 | A10 | 17736628 | G | A | missense_variant | MODERATE | c.898C>T|p.Arg300Cys |
S203 |
| 132319 | BAA10g19300 | A10 | 17736888 | G | A | missense_variant | MODERATE | c.638C>T|p.Pro213Leu |
S130 |
| 132320 | BAA10g19300 | A10 | 17737624 | G | A | intron_variant | MODIFIER | c.522+545C>T| |
S85 |
| 132321 | BAA10g19300 | A10 | 17739250 | C | T | upstream_gene_variant | MODIFIER | c.-560G>A| |
S272 |
| 132322 | BAA10g19300 | A10 | 17739313 | C | T | upstream_gene_variant | MODIFIER | c.-623G>A| |
S267 |
| 132323 | BAA10g19300 | A10 | 17739643 | C | T | upstream_gene_variant | MODIFIER | c.-953G>A| |
S238 |
| 132324 | BAA10g19300 | A10 | 17742870 | C | T | upstream_gene_variant | MODIFIER | c.-4180G>A| |
S301 S304 |
| 132325 | BAA10g19300 | A10 | 17743246 | C | T | upstream_gene_variant | MODIFIER | c.-4556G>A| |
S136 S186 S275 S301 S304 |