| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 68001 | BAA01g35650 | A01 | 23849023 | C | T | downstream_gene_variant | MODIFIER | c.*4211C>T| |
S167 |
| 68002 | BAA01g35650 | A01 | 23849028 | G | A | downstream_gene_variant | MODIFIER | c.*4216G>A| |
S71 |
| 68003 | BAA01g35650 | A01 | 23849123 | G | A | downstream_gene_variant | MODIFIER | c.*4311G>A| |
S176 |
| 68004 | BAA01g35650 | A01 | 23849128 | G | A | downstream_gene_variant | MODIFIER | c.*4316G>A| |
S176 |
| 68005 | BAA01g35650 | A01 | 23849397 | G | A | downstream_gene_variant | MODIFIER | c.*4585G>A| |
S159 S243 |
| 68006 | BAA01g35650 | A01 | 23849553 | G | A | downstream_gene_variant | MODIFIER | c.*4741G>A| |
S163 |
| 68007 | BAA01g35660 | A01 | 23849974 | C | T | downstream_gene_variant | MODIFIER | c.*2076C>T| |
S134 |
| 68008 | BAA01g35660 | A01 | 23851784 | C | T | downstream_gene_variant | MODIFIER | c.*3886C>T| |
S77 |
| 68009 | BAA01g35670 | A01 | 23852030 | C | T | upstream_gene_variant | MODIFIER | c.-4959C>T| |
S47 |
| 68010 | BAA01g35670 | A01 | 23852048 | C | T | upstream_gene_variant | MODIFIER | c.-4941C>T| |
S185 S200 |
| 68011 | BAA01g35670 | A01 | 23852251 | C | T | upstream_gene_variant | MODIFIER | c.-4738C>T| |
S134 |
| 68012 | BAA01g35670 | A01 | 23854217 | G | A | upstream_gene_variant | MODIFIER | c.-2772G>A| |
S74 |
| 68013 | BAA01g35670 | A01 | 23857233 | G | A | missense_variant | MODERATE | c.245G>A|p.Gly82Glu |
S159 S243 |
| 68014 | BAA01g35670 | A01 | 23857632 | C | T | missense_variant | MODERATE | c.644C>T|p.Pro215Leu |
S108 |
| 68015 | BAA01g35670 | A01 | 23857904 | C | T | missense_variant | MODERATE | c.916C>T|p.Pro306Ser |
S233 |
| 68016 | BAA01g35670 | A01 | 23858257 | C | T | missense_variant | MODERATE | c.1180C>T|p.Pro394Ser |
S179 |
| 68017 | BAA01g35670 | A01 | 23858477 | C | T | missense_variant | MODERATE | c.1400C>T|p.Ser467Phe |
S240 |
| 68018 | BAA01g35680 | A01 | 23858585 | G | A | downstream_gene_variant | MODIFIER | c.*4662C>T| |
S275 |
| 68019 | BAA01g35670 | A01 | 23859102 | G | A | missense_variant | MODERATE | c.1769G>A|p.Arg590Lys |
S274 |
| 68020 | BAA01g35670 | A01 | 23859777 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1826-1G>A| |
S74 |
| 68021 | BAA01g35670 | A01 | 23859879 | G | A | missense_variant | MODERATE | c.1927G>A|p.Glu643Lys |
S35 |
| 68022 | BAA01g35680 | A01 | 23859954 | C | T | downstream_gene_variant | MODIFIER | c.*3293G>A| |
S41 |
| 68023 | BAA01g35680 | A01 | 23860026 | G | A | downstream_gene_variant | MODIFIER | c.*3221C>T| |
S17 |
| 68024 | BAA01g35670 | A01 | 23860277 | G | A | downstream_gene_variant | MODIFIER | c.*94G>A| |
S115 S117 S120 S65 S9 |
| 68025 | BAA01g35670 | A01 | 23860369 | G | A | downstream_gene_variant | MODIFIER | c.*186G>A| |
S298 |