| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 164051 | BAA02g10640 | A02 | 4741930 | G | T | intron_variant | MODIFIER | c.628+23G>T| |
S4 |
| 164052 | BAA02g10640 | A02 | 4742087 | C | T | intron_variant | MODIFIER | c.628+180C>T| |
S181 |
| 164053 | BAA02g10640 | A02 | 4744819 | C | T | intron_variant | MODIFIER | c.931-760C>T| |
S218 |
| 164054 | BAA02g10640 | A02 | 4745457 | G | A | intron_variant | MODIFIER | c.931-122G>A| |
S92 |
| 164055 | BAA02g10640 | A02 | 4747402 | C | T | synonymous_variant | LOW | c.2391C>T|p.Gly797Gly |
S128 |
| 164056 | BAA02g10640 | A02 | 4747776 | G | A | intron_variant | MODIFIER | c.2675+90G>A| |
S10 |
| 164057 | BAA02g10640 | A02 | 4748174 | C | T | stop_gained | HIGH | c.2953C>T|p.Gln985* |
S15 S2 S3 S34 S4 S6 |
| 164058 | BAA02g10640 | A02 | 4748610 | C | T | missense_variant | MODERATE | c.3389C>T|p.Thr1130Ile |
S202 |
| 164059 | BAA02g10640 | A02 | 4749230 | G | A | missense_variant | MODERATE | c.3805G>A|p.Gly1269Arg |
S210 S225 |
| 164060 | BAA02g10640 | A02 | 4750852 | C | T | synonymous_variant | LOW | c.4989C>T|p.His1663His |
S104 |
| 164061 | BAA02g10640 | A02 | 4751055 | C | T | missense_variant | MODERATE | c.5192C>T|p.Ser1731Phe |
S129 |
| 164062 | BAA02g10640 | A02 | 4751188 | G | A | synonymous_variant | LOW | c.5325G>A|p.Pro1775Pro |
S162 |
| 164063 | BAA02g10640 | A02 | 4751503 | G | A | synonymous_variant | LOW | c.5640G>A|p.Ala1880Ala |
S197 |
| 164064 | BAA02g10640 | A02 | 4751988 | G | A | downstream_gene_variant | MODIFIER | c.*248G>A| |
S207 |
| 164065 | BAA02g10640 | A02 | 4755886 | G | A | downstream_gene_variant | MODIFIER | c.*4146G>A| |
S98 |
| 164066 | BAA02g10640 | A02 | 4755893 | G | A | downstream_gene_variant | MODIFIER | c.*4153G>A| |
S225 |
| 164067 | BAA02g10650 | A02 | 4756971 | C | T | downstream_gene_variant | MODIFIER | c.*123G>A| |
S123 |
| 164068 | BAA02g10650 | A02 | 4757615 | G | A | missense_variant | MODERATE | c.670C>T|p.Arg224Cys |
S221 |
| 164069 | BAA02g10650 | A02 | 4758599 | C | T | upstream_gene_variant | MODIFIER | c.-315G>A| |
S119 |
| 164070 | BAA02g10650 | A02 | 4761321 | C | T | upstream_gene_variant | MODIFIER | c.-3037G>A| |
S179 |
| 164071 | BAA02g10660 | A02 | 4763661 | T | A | downstream_gene_variant | MODIFIER | c.*87A>T| |
S266 |
| 164072 | BAA02g10660 | A02 | 4763673 | T | A | downstream_gene_variant | MODIFIER | c.*75A>T| |
S266 |
| 164073 | BAA02g10660 | A02 | 4763680 | G | A | downstream_gene_variant | MODIFIER | c.*68C>T| |
S266 |
| 164074 | BAA02g10660 | A02 | 4763790 | G | A | synonymous_variant | LOW | c.1038C>T|p.Phe346Phe |
S153 S166 S257 S263 |
| 164075 | BAA02g10660 | A02 | 4765105 | A | G | upstream_gene_variant | MODIFIER | c.-145T>C| |
S175 |