| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 165451 | BAA02g11650 | A02 | 5264147 | C | T | missense_variant | MODERATE | c.11G>A|p.Arg4His |
S129 |
| 165452 | BAA02g11640 | A02 | 5264163 | C | T | upstream_gene_variant | MODIFIER | c.-1830G>A| |
S272 |
| 165453 | BAA02g11640 | A02 | 5264556 | G | A | upstream_gene_variant | MODIFIER | c.-2223C>T| |
S189 |
| 165454 | BAA02g11640 | A02 | 5265579 | G | A | upstream_gene_variant | MODIFIER | c.-3246C>T| |
S295 |
| 165455 | BAA02g11640 | A02 | 5266561 | G | A | upstream_gene_variant | MODIFIER | c.-4228C>T| |
S146 |
| 165456 | BAA02g11640 | A02 | 5267012 | C | T | upstream_gene_variant | MODIFIER | c.-4679G>A| |
S15 S3 |
| 165457 | BAA02g11660 | A02 | 5267937 | G | A | synonymous_variant | LOW | c.2073C>T|p.Asn691Asn |
S148 S210 S30 S31 |
| 165458 | BAA02g11660 | A02 | 5269573 | G | A | missense_variant | MODERATE | c.1162C>T|p.Pro388Ser |
S295 |
| 165459 | BAA02g11660 | A02 | 5270082 | C | T | missense_variant | MODERATE | c.751G>A|p.Ala251Thr |
S32 |
| 165460 | BAA02g11670 | A02 | 5272210 | C | T | missense_variant | MODERATE | c.2251G>A|p.Asp751Asn |
S275 |
| 165461 | BAA02g11670 | A02 | 5272914 | G | A | missense_variant | MODERATE | c.1835C>T|p.Ser612Phe |
S229 |
| 165462 | BAA02g11670 | A02 | 5273244 | G | A | missense_variant | MODERATE | c.1585C>T|p.Leu529Phe |
S190 |
| 165463 | BAA02g11670 | A02 | 5274623 | C | T | stop_gained | HIGH | c.669G>A|p.Trp223* |
S127 |
| 165464 | BAA02g11670 | A02 | 5274662 | C | T | synonymous_variant | LOW | c.630G>A|p.Pro210Pro |
S250 |
| 165465 | BAA02g11670 | A02 | 5275352 | G | A | synonymous_variant | LOW | c.286C>T|p.Leu96Leu |
S287 |
| 165466 | BAA02g11670 | A02 | 5275502 | C | T | missense_variant | MODERATE | c.136G>A|p.Glu46Lys |
S157 S163 |
| 165467 | BAA02g11670 | A02 | 5275513 | G | A | missense_variant | MODERATE | c.125C>T|p.Ser42Phe |
S165 |
| 165468 | BAA02g11660 | A02 | 5275850 | G | A | upstream_gene_variant | MODIFIER | c.-4694C>T| |
S296 |
| 165469 | BAA02g11670 | A02 | 5276635 | C | T | upstream_gene_variant | MODIFIER | c.-880G>A| |
S234 |
| 165470 | BAA02g11680 | A02 | 5278092 | C | T | missense_variant | MODERATE | c.2351G>A|p.Arg784Lys |
S177 S195 |
| 165471 | BAA02g11680 | A02 | 5278107 | G | A | missense_variant | MODERATE | c.2336C>T|p.Ser779Phe |
S113 |
| 165472 | BAA02g11680 | A02 | 5278682 | G | A | splice_region_variant&intron_variant | LOW | c.1948+4C>T| |
S170 |
| 165473 | BAA02g11680 | A02 | 5278712 | A | T | missense_variant | MODERATE | c.1922T>A|p.Leu641Gln |
S120 |
| 165474 | BAA02g11670 | A02 | 5279348 | C | T | upstream_gene_variant | MODIFIER | c.-3593G>A| |
S196 |
| 165475 | BAA02g11670 | A02 | 5279807 | G | A | upstream_gene_variant | MODIFIER | c.-4052C>T| |
S232 |