| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 178451 | BAA02g19380 | A02 | 10044543 | C | T | missense_variant | MODERATE | c.97C>T|p.Leu33Phe |
S178 |
| 178452 | BAA02g19380 | A02 | 10044717 | C | T | synonymous_variant | LOW | c.271C>T|p.Leu91Leu |
S266 |
| 178453 | BAA02g19380 | A02 | 10045202 | C | T | synonymous_variant | LOW | c.756C>T|p.Leu252Leu |
S186 |
| 178454 | BAA02g19380 | A02 | 10045652 | G | A | downstream_gene_variant | MODIFIER | c.*111G>A| |
S132 S215 S89 |
| 178455 | BAA02g19390 | A02 | 10045983 | C | T | missense_variant | MODERATE | c.617G>A|p.Gly206Glu |
S135 |
| 178456 | BAA02g19390 | A02 | 10049256 | C | T | upstream_gene_variant | MODIFIER | c.-2657G>A| |
S198 |
| 178457 | BAA02g19400 | A02 | 10052247 | G | A | upstream_gene_variant | MODIFIER | c.-888G>A| |
S276 |
| 178458 | BAA02g19400 | A02 | 10053152 | C | T | synonymous_variant | LOW | c.18C>T|p.Leu6Leu |
S6 |
| 178459 | BAA02g19400 | A02 | 10053220 | G | A | missense_variant | MODERATE | c.86G>A|p.Gly29Glu |
S293 |
| 178460 | BAA02g19400 | A02 | 10053327 | G | A | intron_variant | MODIFIER | c.110-12G>A| |
S62 |
| 178461 | BAA02g19400 | A02 | 10054196 | G | A | intron_variant | MODIFIER | c.584+43G>A| |
S13 S140 S168 S279 S64 |
| 178462 | BAA02g19400 | A02 | 10054740 | G | A | missense_variant&splice_region_variant | MODERATE | c.731G>A|p.Arg244Lys |
S240 |
| 178463 | BAA02g19400 | A02 | 10055119 | C | T | intron_variant | MODIFIER | c.800+310C>T| |
S121 |
| 178464 | BAA02g19400 | A02 | 10055151 | G | A | intron_variant | MODIFIER | c.800+342G>A| |
S5 |
| 178465 | BAA02g19400 | A02 | 10055613 | G | A | intron_variant | MODIFIER | c.801-260G>A| |
S126 |
| 178466 | BAA02g19400 | A02 | 10056690 | C | T | splice_region_variant&intron_variant | LOW | c.1083-7C>T| |
S2 |
| 178467 | BAA02g19400 | A02 | 10056754 | C | T | synonymous_variant | LOW | c.1140C>T|p.Asn380Asn |
S80 |
| 178468 | BAA02g19400 | A02 | 10057293 | G | A | intron_variant | MODIFIER | c.1149-286G>A| |
S116 |
| 178469 | BAA02g19400 | A02 | 10060092 | G | A | intron_variant | MODIFIER | c.2088+1157G>A| |
S303 |
| 178470 | BAA02g19400 | A02 | 10061514 | T | C | intron_variant | MODIFIER | c.2089-146T>C| |
S50 |
| 178471 | BAA02g19400 | A02 | 10061980 | G | A | missense_variant | MODERATE | c.2311G>A|p.Asp771Asn |
S229 |
| 178472 | BAA02g19410 | A02 | 10065316 | C | T | upstream_gene_variant | MODIFIER | c.-4162C>T| |
S138 |
| 178473 | BAA02g19410 | A02 | 10065363 | C | T | upstream_gene_variant | MODIFIER | c.-4115C>T| |
S216 S241 S265 S39 |
| 178474 | BAA02g19410 | A02 | 10065704 | C | T | upstream_gene_variant | MODIFIER | c.-3774C>T| |
S124 |
| 178475 | BAA02g19410 | A02 | 10065762 | C | T | upstream_gene_variant | MODIFIER | c.-3716C>T| |
S277 |