| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 73251 | BAA01g38390 | A01 | 25594066 | C | T | upstream_gene_variant | MODIFIER | c.-3202C>T| |
S240 |
| 73252 | BAA01g38390 | A01 | 25594211 | C | T | upstream_gene_variant | MODIFIER | c.-3057C>T| |
S203 |
| 73253 | BAA01g38390 | A01 | 25594882 | G | A | upstream_gene_variant | MODIFIER | c.-2386G>A| |
S60 |
| 73254 | BAA01g38390 | A01 | 25595776 | C | T | upstream_gene_variant | MODIFIER | c.-1492C>T| |
S186 |
| 73255 | BAA01g38390 | A01 | 25597330 | C | T | synonymous_variant | LOW | c.63C>T|p.Phe21Phe |
S295 |
| 73256 | BAA01g38390 | A01 | 25597362 | C | T | intron_variant | MODIFIER | c.80+15C>T| |
S56 |
| 73257 | BAA01g38390 | A01 | 25597557 | G | A | synonymous_variant | LOW | c.159G>A|p.Val53Val |
S20 |
| 73258 | BAA01g38390 | A01 | 25597574 | G | A | missense_variant | MODERATE | c.176G>A|p.Gly59Glu |
S66 |
| 73259 | BAA01g38390 | A01 | 25597792 | G | A | missense_variant | MODERATE | c.328G>A|p.Glu110Lys |
S132 S137 S138 S215 S89 |
| 73260 | BAA01g38390 | A01 | 25598443 | C | T | missense_variant | MODERATE | c.764C>T|p.Pro255Leu |
S8 |
| 73261 | BAA01g38390 | A01 | 25598935 | G | A | synonymous_variant | LOW | c.1056G>A|p.Leu352Leu |
S70 |
| 73262 | BAA01g38400 | A01 | 25599036 | G | A | upstream_gene_variant | MODIFIER | c.-4753G>A| |
S105 S106 |
| 73263 | BAA01g38400 | A01 | 25600214 | T | G | upstream_gene_variant | MODIFIER | c.-3575T>G| |
S196 S34 S71 S96 |
| 73264 | BAA01g38390 | A01 | 25601256 | C | T | stop_gained | HIGH | c.2203C>T|p.Arg735* |
S168 |
| 73265 | BAA01g38390 | A01 | 25601807 | G | A | missense_variant | MODERATE | c.2577G>A|p.Met859Ile |
S105 S106 |
| 73266 | BAA01g38390 | A01 | 25601994 | G | A | missense_variant | MODERATE | c.2686G>A|p.Asp896Asn |
S60 |
| 73267 | BAA01g38390 | A01 | 25602192 | G | A | missense_variant | MODERATE | c.2800G>A|p.Ala934Thr |
S38 |
| 73268 | BAA01g38390 | A01 | 25602379 | C | T | missense_variant | MODERATE | c.2908C>T|p.Pro970Ser |
S75 S81 |
| 73269 | BAA01g38390 | A01 | 25602416 | G | A | missense_variant | MODERATE | c.2945G>A|p.Arg982Gln |
S45 |
| 73270 | BAA01g38400 | A01 | 25603181 | C | T | upstream_gene_variant | MODIFIER | c.-608C>T| |
S19 |
| 73271 | BAA01g38400 | A01 | 25603838 | T | C | missense_variant | MODERATE | c.50T>C|p.Leu17Pro |
S62 |
| 73272 | BAA01g38400 | A01 | 25604102 | C | T | missense_variant | MODERATE | c.314C>T|p.Ala105Val |
S277 |
| 73273 | BAA01g38400 | A01 | 25604134 | G | A | missense_variant | MODERATE | c.346G>A|p.Ala116Thr |
S278 |
| 73274 | BAA01g38410 | A01 | 25604606 | G | A | upstream_gene_variant | MODIFIER | c.-4651G>A| |
S294 |
| 73275 | BAA01g38410 | A01 | 25604694 | G | A | upstream_gene_variant | MODIFIER | c.-4563G>A| |
S278 |