| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 163601 | BAA02g10270 | A02 | 4566024 | C | T | missense_variant | MODERATE | c.784G>A|p.Glu262Lys |
S218 |
| 163602 | BAA02g10270 | A02 | 4566123 | C | T | missense_variant | MODERATE | c.685G>A|p.Asp229Asn |
S277 |
| 163603 | BAA02g10270 | A02 | 4566356 | C | T | missense_variant | MODERATE | c.452G>A|p.Gly151Asp |
S127 |
| 163604 | BAA02g10270 | A02 | 4566422 | C | T | missense_variant | MODERATE | c.386G>A|p.Arg129Lys |
S90 |
| 163605 | BAA02g10260 | A02 | 4567421 | G | A | upstream_gene_variant | MODIFIER | c.-3494C>T| |
S231 S9 |
| 163606 | BAA02g10260 | A02 | 4567920 | C | T | upstream_gene_variant | MODIFIER | c.-3993G>A| |
S15 S3 |
| 163607 | BAA02g10280 | A02 | 4568232 | C | T | synonymous_variant | LOW | c.972G>A|p.Arg324Arg |
S135 |
| 163608 | BAA02g10280 | A02 | 4568554 | C | T | missense_variant | MODERATE | c.719G>A|p.Gly240Glu |
S183 S198 |
| 163609 | BAA02g10270 | A02 | 4569427 | C | T | upstream_gene_variant | MODIFIER | c.-2620G>A| |
S32 |
| 163610 | BAA02g10280 | A02 | 4569521 | G | A | synonymous_variant | LOW | c.75C>T|p.Leu25Leu |
S279 |
| 163611 | BAA02g10270 | A02 | 4570140 | G | A | upstream_gene_variant | MODIFIER | c.-3333C>T| |
S25 |
| 163612 | BAA02g10270 | A02 | 4570372 | G | A | upstream_gene_variant | MODIFIER | c.-3565C>T| |
S305 |
| 163613 | BAA02g10270 | A02 | 4570378 | C | T | upstream_gene_variant | MODIFIER | c.-3571G>A| |
S270 |
| 163614 | BAA02g10270 | A02 | 4571014 | C | T | upstream_gene_variant | MODIFIER | c.-4207G>A| |
S243 |
| 163615 | BAA02g10300 | A02 | 4572335 | G | A | missense_variant | MODERATE | c.166G>A|p.Glu56Lys |
S80 |
| 163616 | BAA02g10300 | A02 | 4572539 | C | T | missense_variant | MODERATE | c.370C>T|p.His124Tyr |
S272 |
| 163617 | BAA02g10280 | A02 | 4572951 | C | T | upstream_gene_variant | MODIFIER | c.-3356G>A| |
S46 |
| 163618 | BAA02g10310 | A02 | 4573541 | C | T | missense_variant | MODERATE | c.706G>A|p.Asp236Asn |
S257 |
| 163619 | BAA02g10310 | A02 | 4573694 | G | A | synonymous_variant | LOW | c.553C>T|p.Leu185Leu |
S302 |
| 163620 | BAA02g10310 | A02 | 4573700 | C | T | missense_variant | MODERATE | c.547G>A|p.Glu183Lys |
S250 |
| 163621 | BAA02g10310 | A02 | 4573702 | C | T | missense_variant | MODERATE | c.545G>A|p.Gly182Glu |
S211 S227 |
| 163622 | BAA02g10310 | A02 | 4573943 | G | A | missense_variant | MODERATE | c.304C>T|p.Arg102Cys |
S59 |
| 163623 | BAA02g10280 | A02 | 4574516 | C | T | upstream_gene_variant | MODIFIER | c.-4921G>A| |
S240 |
| 163624 | BAA02g10320 | A02 | 4577659 | G | A | synonymous_variant | LOW | c.213C>T|p.Ser71Ser |
S79 S91 |
| 163625 | BAA02g10310 | A02 | 4578542 | C | T | upstream_gene_variant | MODIFIER | c.-4296G>A| |
S42 |