| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 72401 | BAA01g37870 | A01 | 25307248 | C | T | upstream_gene_variant | MODIFIER | c.-1376C>T| |
S111 |
| 72402 | BAA01g37870 | A01 | 25307354 | C | T | upstream_gene_variant | MODIFIER | c.-1270C>T| |
S80 |
| 72403 | BAA01g37870 | A01 | 25308167 | G | A | upstream_gene_variant | MODIFIER | c.-457G>A| |
S1 S90 |
| 72404 | BAA01g37870 | A01 | 25308560 | C | T | upstream_gene_variant | MODIFIER | c.-64C>T| |
S183 S198 |
| 72405 | BAA01g37870 | A01 | 25308681 | C | T | missense_variant | MODERATE | c.58C>T|p.Leu20Phe |
S305 |
| 72406 | BAA01g37880 | A01 | 25309034 | G | A | upstream_gene_variant | MODIFIER | c.-704G>A| |
S126 |
| 72407 | BAA01g37870 | A01 | 25309161 | C | T | missense_variant | MODERATE | c.298C>T|p.Leu100Phe |
S182 |
| 72408 | BAA01g37880 | A01 | 25309537 | C | T | upstream_gene_variant | MODIFIER | c.-201C>T| |
S28 |
| 72409 | BAA01g37880 | A01 | 25309803 | C | T | synonymous_variant | LOW | c.66C>T|p.His22His |
S167 |
| 72410 | BAA01g37880 | A01 | 25310135 | G | A | missense_variant | MODERATE | c.398G>A|p.Gly133Glu |
S173 |
| 72411 | BAA01g37880 | A01 | 25310387 | G | A | missense_variant | MODERATE | c.650G>A|p.Arg217Lys |
S45 |
| 72412 | BAA01g37880 | A01 | 25310393 | G | A | missense_variant | MODERATE | c.656G>A|p.Gly219Asp |
S105 |
| 72413 | BAA01g37880 | A01 | 25310835 | G | A | synonymous_variant | LOW | c.1098G>A|p.Gln366Gln |
S122 |
| 72414 | BAA01g37880 | A01 | 25311011 | C | T | missense_variant | MODERATE | c.1274C>T|p.Ala425Val |
S115 |
| 72415 | BAA01g37890 | A01 | 25311780 | G | A | upstream_gene_variant | MODIFIER | c.-340G>A| |
S263 |
| 72416 | BAA01g37890 | A01 | 25311822 | C | T | upstream_gene_variant | MODIFIER | c.-298C>T| |
S85 |
| 72417 | BAA01g37890 | A01 | 25312519 | G | A | synonymous_variant | LOW | c.300G>A|p.Lys100Lys |
S281 |
| 72418 | BAA01g37890 | A01 | 25313114 | C | T | missense_variant | MODERATE | c.895C>T|p.Leu299Phe |
S288 |
| 72419 | BAA01g37890 | A01 | 25313543 | C | T | missense_variant | MODERATE | c.1324C>T|p.Leu442Phe |
S179 |
| 72420 | BAA01g37880 | A01 | 25315236 | G | A | downstream_gene_variant | MODIFIER | c.*3531G>A| |
S297 |
| 72421 | BAA01g37880 | A01 | 25315348 | C | T | downstream_gene_variant | MODIFIER | c.*3643C>T| |
S302 |
| 72422 | BAA01g37880 | A01 | 25316024 | G | A | downstream_gene_variant | MODIFIER | c.*4319G>A| |
S246 |
| 72423 | BAA01g37890 | A01 | 25316757 | G | A | downstream_gene_variant | MODIFIER | c.*2846G>A| |
S159 S243 |
| 72424 | BAA01g37890 | A01 | 25317007 | C | T | downstream_gene_variant | MODIFIER | c.*3096C>T| |
S205 |
| 72425 | BAA01g37890 | A01 | 25317163 | G | A | downstream_gene_variant | MODIFIER | c.*3252G>A| |
S155 |