| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 60401 | BAA01g32220 | A01 | 21140117 | C | T | missense_variant | MODERATE | c.1756G>A|p.Asp586Asn |
S192 |
| 60402 | BAA01g32220 | A01 | 21140214 | G | A | synonymous_variant | LOW | c.1659C>T|p.Ala553Ala |
S260 |
| 60403 | BAA01g32220 | A01 | 21140580 | C | T | splice_donor_variant&intron_variant | HIGH | c.1365+1G>A| |
S150 |
| 60404 | BAA01g32220 | A01 | 21140808 | C | T | missense_variant | MODERATE | c.1216G>A|p.Ala406Thr |
S256 |
| 60405 | BAA01g32220 | A01 | 21141951 | G | A | missense_variant | MODERATE | c.770C>T|p.Ser257Phe |
S302 |
| 60406 | BAA01g32230 | A01 | 21142144 | C | T | downstream_gene_variant | MODIFIER | c.*3013G>A| |
S150 |
| 60407 | BAA01g32220 | A01 | 21143121 | G | A | missense_variant | MODERATE | c.187C>T|p.Pro63Ser |
S257 |
| 60408 | BAA01g32230 | A01 | 21145352 | G | A | synonymous_variant | LOW | c.1332C>T|p.Asn444Asn |
S143 |
| 60409 | BAA01g32230 | A01 | 21145370 | C | T | synonymous_variant | LOW | c.1314G>A|p.Gln438Gln |
S200 |
| 60410 | BAA01g32230 | A01 | 21145417 | G | A | missense_variant | MODERATE | c.1267C>T|p.Arg423Cys |
S62 |
| 60411 | BAA01g32230 | A01 | 21145476 | C | T | missense_variant | MODERATE | c.1208G>A|p.Gly403Glu |
S178 |
| 60412 | BAA01g32220 | A01 | 21145877 | G | A | upstream_gene_variant | MODIFIER | c.-2570C>T| |
S172 S217 |
| 60413 | BAA01g32230 | A01 | 21146090 | G | A | synonymous_variant | LOW | c.846C>T|p.Pro282Pro |
S161 |
| 60414 | BAA01g32220 | A01 | 21146207 | G | A | upstream_gene_variant | MODIFIER | c.-2900C>T| |
S221 |
| 60415 | BAA01g32220 | A01 | 21146245 | C | T | upstream_gene_variant | MODIFIER | c.-2938G>A| |
S136 |
| 60416 | BAA01g32220 | A01 | 21147795 | C | T | upstream_gene_variant | MODIFIER | c.-4488G>A| |
S48 |
| 60417 | BAA01g32230 | A01 | 21150650 | C | T | upstream_gene_variant | MODIFIER | c.-2899G>A| |
S66 S67 |
| 60418 | BAA01g32240 | A01 | 21153489 | G | A | missense_variant | MODERATE | c.3089C>T|p.Ser1030Phe |
S121 |
| 60419 | BAA01g32240 | A01 | 21154998 | C | T | synonymous_variant | LOW | c.2448G>A|p.Glu816Glu |
S47 |
| 60420 | BAA01g32240 | A01 | 21155532 | C | T | missense_variant | MODERATE | c.2095G>A|p.Asp699Asn |
S239 |
| 60421 | BAA01g32240 | A01 | 21155989 | G | A | intron_variant | MODIFIER | c.1948-29C>T| |
S124 |
| 60422 | BAA01g32240 | A01 | 21157727 | A | G | synonymous_variant | LOW | c.1390T>C|p.Leu464Leu |
S180 |
| 60423 | BAA01g32240 | A01 | 21158629 | G | A | missense_variant | MODERATE | c.932C>T|p.Pro311Leu |
S193 |
| 60424 | BAA01g32240 | A01 | 21158635 | G | A | missense_variant | MODERATE | c.926C>T|p.Pro309Leu |
S12 |
| 60425 | BAA01g32240 | A01 | 21158975 | C | T | splice_region_variant&intron_variant | LOW | c.819+5G>A| |
S201 |