| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 138601 | BAA10g24070 | A10 | 19970665 | G | A | missense_variant | MODERATE | c.175C>T|p.Pro59Ser |
S173 |
| 138602 | BAA10g24070 | A10 | 19970789 | C | T | synonymous_variant | LOW | c.51G>A|p.Lys17Lys |
S23 |
| 138603 | BAA10g24070 | A10 | 19970933 | G | A | upstream_gene_variant | MODIFIER | c.-94C>T| |
S15 S3 |
| 138604 | BAA10g24080 | A10 | 19971662 | C | T | missense_variant | MODERATE | c.668G>A|p.Ser223Asn |
S187 |
| 138605 | BAA10g24070 | A10 | 19973018 | G | A | upstream_gene_variant | MODIFIER | c.-2179C>T| |
S172 S217 |
| 138606 | BAA10g24070 | A10 | 19974498 | G | A | upstream_gene_variant | MODIFIER | c.-3659C>T| |
S105 |
| 138607 | BAA10g24070 | A10 | 19974761 | G | A | upstream_gene_variant | MODIFIER | c.-3922C>T| |
S127 |
| 138608 | BAA10g24070 | A10 | 19975576 | G | A | upstream_gene_variant | MODIFIER | c.-4737C>T| |
S138 |
| 138609 | BAA10g24080 | A10 | 19976006 | G | A | upstream_gene_variant | MODIFIER | c.-3592C>T| |
S273 |
| 138610 | BAA10g24090 | A10 | 19976583 | C | T | missense_variant | MODERATE | c.10G>A|p.Val4Met |
S283 |
| 138611 | BAA10g24090 | A10 | 19978389 | G | A | upstream_gene_variant | MODIFIER | c.-1797C>T| |
S273 |
| 138612 | BAA10g24100 | A10 | 19979133 | G | A | synonymous_variant | LOW | c.1191C>T|p.Leu397Leu |
S241 |
| 138613 | BAA10g24100 | A10 | 19980466 | C | T | synonymous_variant | LOW | c.297G>A|p.Arg99Arg |
S54 |
| 138614 | BAA10g24100 | A10 | 19980655 | C | T | missense_variant | MODERATE | c.185G>A|p.Ser62Asn |
S119 |
| 138615 | BAA10g24100 | A10 | 19982595 | G | A | upstream_gene_variant | MODIFIER | c.-1635C>T| |
S265 |
| 138616 | BAA10g24100 | A10 | 19985431 | G | A | upstream_gene_variant | MODIFIER | c.-4471C>T| |
S64 |
| 138617 | BAA10g24110 | A10 | 19986487 | C | T | downstream_gene_variant | MODIFIER | c.*2043G>A| |
S25 |
| 138618 | BAA10g24110 | A10 | 19987947 | C | T | downstream_gene_variant | MODIFIER | c.*583G>A| |
S47 |
| 138619 | BAA10g24110 | A10 | 19988037 | G | A | downstream_gene_variant | MODIFIER | c.*493C>T| |
S160 |
| 138620 | BAA10g24110 | A10 | 19988347 | G | A | downstream_gene_variant | MODIFIER | c.*183C>T| |
S178 |
| 138621 | BAA10g24110 | A10 | 19989099 | C | T | missense_variant | MODERATE | c.1384G>A|p.Gly462Arg |
S302 |
| 138622 | BAA10g24110 | A10 | 19989232 | C | T | synonymous_variant | LOW | c.1251G>A|p.Arg417Arg |
S36 |
| 138623 | BAA10g24110 | A10 | 19990511 | G | A | upstream_gene_variant | MODIFIER | c.-29C>T| |
S198 |
| 138624 | BAA10g24110 | A10 | 19990729 | C | T | upstream_gene_variant | MODIFIER | c.-247G>A| |
S204 |
| 138625 | BAA10g24110 | A10 | 19991716 | C | T | upstream_gene_variant | MODIFIER | c.-1234G>A| |
S13 |