| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 164951 | BAA02g11260 | A02 | 5079840 | C | T | synonymous_variant | LOW | c.588C>T|p.Val196Val |
S9 |
| 164952 | BAA02g11260 | A02 | 5079997 | G | A | missense_variant | MODERATE | c.745G>A|p.Ala249Thr |
S177 |
| 164953 | BAA02g11260 | A02 | 5082346 | G | A | downstream_gene_variant | MODIFIER | c.*1492G>A| |
S197 |
| 164954 | BAA02g11270 | A02 | 5082864 | G | A | missense_variant | MODERATE | c.526C>T|p.His176Tyr |
S139 |
| 164955 | BAA02g11270 | A02 | 5083851 | G | A | upstream_gene_variant | MODIFIER | c.-274C>T| |
S295 |
| 164956 | BAA02g11270 | A02 | 5084394 | G | A | upstream_gene_variant | MODIFIER | c.-817C>T| |
S150 |
| 164957 | BAA02g11270 | A02 | 5086490 | G | A | upstream_gene_variant | MODIFIER | c.-2913C>T| |
S247 |
| 164958 | BAA02g11270 | A02 | 5086855 | G | A | upstream_gene_variant | MODIFIER | c.-3278C>T| |
S298 |
| 164959 | BAA02g11270-BAA02g11280 | A02 | 5088941 | G | A | intergenic_region | MODIFIER | n.5088941G>A| |
S86 |
| 164960 | BAA02g11270-BAA02g11280 | A02 | 5089161 | G | A | intergenic_region | MODIFIER | n.5089161G>A| |
S210 |
| 164961 | BAA02g11270-BAA02g11280 | A02 | 5089634 | G | A | intergenic_region | MODIFIER | n.5089634G>A| |
S156 |
| 164962 | BAA02g11270-BAA02g11280 | A02 | 5090534 | C | T | intergenic_region | MODIFIER | n.5090534C>T| |
S1 S90 |
| 164963 | BAA02g11270-BAA02g11280 | A02 | 5091550 | C | T | intergenic_region | MODIFIER | n.5091550C>T| |
S104 |
| 164964 | BAA02g11280 | A02 | 5092266 | G | A | upstream_gene_variant | MODIFIER | c.-4932G>A| |
S187 |
| 164965 | BAA02g11280 | A02 | 5092941 | C | T | upstream_gene_variant | MODIFIER | c.-4257C>T| |
S182 |
| 164966 | BAA02g11280 | A02 | 5093571 | G | A | upstream_gene_variant | MODIFIER | c.-3627G>A| |
S229 |
| 164967 | BAA02g11280 | A02 | 5094604 | C | T | upstream_gene_variant | MODIFIER | c.-2594C>T| |
S249 |
| 164968 | BAA02g11280 | A02 | 5094738 | T | G | upstream_gene_variant | MODIFIER | c.-2460T>G| |
S17 |
| 164969 | BAA02g11280 | A02 | 5094848 | G | A | upstream_gene_variant | MODIFIER | c.-2350G>A| |
S205 |
| 164970 | BAA02g11280 | A02 | 5095133 | C | T | upstream_gene_variant | MODIFIER | c.-2065C>T| |
S186 |
| 164971 | BAA02g11280 | A02 | 5095435 | C | T | upstream_gene_variant | MODIFIER | c.-1763C>T| |
S123 S99 |
| 164972 | BAA02g11280 | A02 | 5095574 | G | A | upstream_gene_variant | MODIFIER | c.-1624G>A| |
S282 |
| 164973 | BAA02g11280 | A02 | 5095920 | G | A | upstream_gene_variant | MODIFIER | c.-1278G>A| |
S229 |
| 164974 | BAA02g11280 | A02 | 5097870 | G | A | missense_variant | MODERATE | c.445G>A|p.Asp149Asn |
S204 |
| 164975 | BAA02g11280 | A02 | 5098673 | G | A | downstream_gene_variant | MODIFIER | c.*257G>A| |
S206 S26 |