| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 195101 | BAA02g28360 | A02 | 15932945 | C | T | missense_variant | MODERATE | c.5582C>T|p.Thr1861Ile |
S65 |
| 195102 | BAA02g28360 | A02 | 15933478 | G | A | intron_variant | MODIFIER | c.5773-96G>A| |
S143 |
| 195103 | BAA02g28360 | A02 | 15933720 | G | A | intron_variant | MODIFIER | c.5879+40G>A| |
S302 |
| 195104 | BAA02g28360 | A02 | 15934585 | C | T | missense_variant | MODERATE | c.6293C>T|p.Ser2098Leu |
S11 |
| 195105 | BAA02g28360 | A02 | 15935732 | C | T | synonymous_variant | LOW | c.6825C>T|p.Ile2275Ile |
S182 |
| 195106 | BAA02g28360 | A02 | 15936128 | G | A | intron_variant | MODIFIER | c.7027-38G>A| |
S95 |
| 195107 | BAA02g28360 | A02 | 15936757 | C | T | intron_variant | MODIFIER | c.7405-14C>T| |
S144 |
| 195108 | BAA02g28360 | A02 | 15937020 | C | T | intron_variant | MODIFIER | c.7588-25C>T| |
S152 |
| 195109 | BAA02g28360 | A02 | 15937730 | G | A | downstream_gene_variant | MODIFIER | c.*91G>A| |
S256 |
| 195110 | BAA02g28360 | A02 | 15937861 | C | T | downstream_gene_variant | MODIFIER | c.*222C>T| |
S292 |
| 195111 | BAA02g28370 | A02 | 15941580 | C | T | upstream_gene_variant | MODIFIER | c.-3471C>T| |
S6 |
| 195112 | BAA02g28370 | A02 | 15942134 | C | T | upstream_gene_variant | MODIFIER | c.-2917C>T| |
S118 |
| 195113 | BAA02g28370 | A02 | 15944337 | G | A | upstream_gene_variant | MODIFIER | c.-714G>A| |
S13 S140 S279 S64 |
| 195114 | BAA02g28370 | A02 | 15944783 | G | A | upstream_gene_variant | MODIFIER | c.-268G>A| |
S298 |
| 195115 | BAA02g28380 | A02 | 15946229 | G | A | downstream_gene_variant | MODIFIER | c.*2161C>T| |
S47 |
| 195116 | BAA02g28380 | A02 | 15946767 | G | A | downstream_gene_variant | MODIFIER | c.*1623C>T| |
S125 |
| 195117 | BAA02g28380 | A02 | 15946768 | C | T | downstream_gene_variant | MODIFIER | c.*1622G>A| |
S139 |
| 195118 | BAA02g28370 | A02 | 15946853 | G | A | synonymous_variant | LOW | c.384G>A|p.Val128Val |
S103 |
| 195119 | BAA02g28370 | A02 | 15947639 | C | T | missense_variant | MODERATE | c.791C>T|p.Ser264Phe |
S305 |
| 195120 | BAA02g28380 | A02 | 15948433 | C | T | missense_variant | MODERATE | c.818G>A|p.Arg273Lys |
S140 |
| 195121 | BAA02g28380 | A02 | 15948863 | G | A | missense_variant | MODERATE | c.388C>T|p.Pro130Ser |
S79 S91 |
| 195122 | BAA02g28380 | A02 | 15949254 | G | A | upstream_gene_variant | MODIFIER | c.-4C>T| |
S207 |
| 195123 | BAA02g28380 | A02 | 15949262 | G | A | upstream_gene_variant | MODIFIER | c.-12C>T| |
S297 S72 S78 |
| 195124 | BAA02g28380 | A02 | 15949323 | C | T | upstream_gene_variant | MODIFIER | c.-73G>A| |
S46 |
| 195125 | BAA02g28380 | A02 | 15950056 | C | T | upstream_gene_variant | MODIFIER | c.-806G>A| |
S218 |