| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 155501 | BAA02g03610 | A02 | 1596507 | C | G | upstream_gene_variant | MODIFIER | c.-475C>G| |
S182 |
| 155502 | BAA02g03610 | A02 | 1596551 | C | T | upstream_gene_variant | MODIFIER | c.-431C>T| |
S75 |
| 155503 | BAA02g03610 | A02 | 1597006 | G | A | missense_variant | MODERATE | c.25G>A|p.Val9Ile |
S209 |
| 155504 | BAA02g03610 | A02 | 1597188 | C | T | synonymous_variant | LOW | c.207C>T|p.Asn69Asn |
S183 S198 |
| 155505 | BAA02g03610 | A02 | 1597190 | G | A | missense_variant | MODERATE | c.209G>A|p.Arg70His |
S45 |
| 155506 | BAA02g03620 | A02 | 1597457 | G | A | upstream_gene_variant | MODIFIER | c.-2308G>A| |
S74 |
| 155507 | BAA02g03620 | A02 | 1597542 | C | T | upstream_gene_variant | MODIFIER | c.-2223C>T| |
S272 |
| 155508 | BAA02g03610 | A02 | 1597841 | C | T | missense_variant | MODERATE | c.449C>T|p.Ala150Val |
S124 |
| 155509 | BAA02g03610 | A02 | 1598058 | C | T | synonymous_variant | LOW | c.666C>T|p.Ile222Ile |
S104 |
| 155510 | BAA02g03620 | A02 | 1598475 | C | T | upstream_gene_variant | MODIFIER | c.-1290C>T| |
S46 |
| 155511 | BAA02g03610 | A02 | 1598919 | C | T | missense_variant | MODERATE | c.1190C>T|p.Ser397Leu |
S61 |
| 155512 | BAA02g03620 | A02 | 1599256 | G | A | upstream_gene_variant | MODIFIER | c.-509G>A| |
S177 |
| 155513 | BAA02g03620 | A02 | 1599294 | G | A | upstream_gene_variant | MODIFIER | c.-471G>A| |
S207 |
| 155514 | BAA02g03610 | A02 | 1599935 | G | A | downstream_gene_variant | MODIFIER | c.*721G>A| |
S26 |
| 155515 | BAA02g03630 | A02 | 1601490 | G | A | upstream_gene_variant | MODIFIER | c.-4998G>A| |
S95 |
| 155516 | BAA02g03630 | A02 | 1601506 | G | A | upstream_gene_variant | MODIFIER | c.-4982G>A| |
S293 |
| 155517 | BAA02g03630 | A02 | 1601932 | G | A | upstream_gene_variant | MODIFIER | c.-4556G>A| |
S145 S192 |
| 155518 | BAA02g03630 | A02 | 1603555 | C | T | upstream_gene_variant | MODIFIER | c.-2933C>T| |
S178 |
| 155519 | BAA02g03630 | A02 | 1604918 | G | A | upstream_gene_variant | MODIFIER | c.-1570G>A| |
S131 |
| 155520 | BAA02g03630 | A02 | 1605165 | C | T | upstream_gene_variant | MODIFIER | c.-1323C>T| |
S157 |
| 155521 | BAA02g03630 | A02 | 1605665 | C | T | upstream_gene_variant | MODIFIER | c.-823C>T| |
S38 |
| 155522 | BAA02g03640 | A02 | 1608067 | C | T | upstream_gene_variant | MODIFIER | c.-831C>T| |
S219 |
| 155523 | BAA02g03640 | A02 | 1608594 | G | A | upstream_gene_variant | MODIFIER | c.-304G>A| |
S288 |
| 155524 | BAA02g03640 | A02 | 1609160 | G | T | missense_variant | MODERATE | c.198G>T|p.Lys66Asn |
S157 |
| 155525 | BAA02g03630 | A02 | 1611074 | G | A | downstream_gene_variant | MODIFIER | c.*4419G>A| |
S157 S166 S167 S236 S262 |