| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 90301 | BAA10g00430-BAA10g00440 | A10 | 189470 | T | A | intergenic_region | MODIFIER | n.189470T>A| |
S54 |
| 90302 | BAA10g00430-BAA10g00440 | A10 | 190047 | C | T | intergenic_region | MODIFIER | n.190047C>T| |
S247 |
| 90303 | BAA10g00430-BAA10g00440 | A10 | 192789 | G | A | intergenic_region | MODIFIER | n.192789G>A| |
S94 |
| 90304 | BAA10g00430-BAA10g00440 | A10 | 192848 | G | A | intergenic_region | MODIFIER | n.192848G>A| |
S95 |
| 90305 | BAA10g00430-BAA10g00440 | A10 | 193108 | C | T | intergenic_region | MODIFIER | n.193108C>T| |
S42 |
| 90306 | BAA10g00430-BAA10g00440 | A10 | 193308 | C | T | intergenic_region | MODIFIER | n.193308C>T| |
S143 |
| 90307 | BAA10g00430-BAA10g00440 | A10 | 193421 | C | T | intergenic_region | MODIFIER | n.193421C>T| |
S165 |
| 90308 | BAA10g00440 | A10 | 198974 | C | T | downstream_gene_variant | MODIFIER | c.*4152G>A| |
S31 |
| 90309 | BAA10g00440 | A10 | 199562 | C | T | downstream_gene_variant | MODIFIER | c.*3564G>A| |
S152 |
| 90310 | BAA10g00440 | A10 | 201915 | G | A | downstream_gene_variant | MODIFIER | c.*1211C>T| |
S76 |
| 90311 | BAA10g00440 | A10 | 204798 | C | T | synonymous_variant | LOW | c.723G>A|p.Glu241Glu |
S61 |
| 90312 | BAA10g00450 | A10 | 205963 | C | T | downstream_gene_variant | MODIFIER | c.*4071G>A| |
S286 |
| 90313 | BAA10g00440 | A10 | 207418 | C | T | missense_variant&splice_region_variant | MODERATE | c.146G>A|p.Gly49Glu |
S116 |
| 90314 | BAA10g00440 | A10 | 208143 | G | A | upstream_gene_variant | MODIFIER | c.-424C>T| |
S115 |
| 90315 | BAA10g00440 | A10 | 208902 | G | A | upstream_gene_variant | MODIFIER | c.-1183C>T| |
S136 |
| 90316 | BAA10g00440 | A10 | 208932 | G | A | upstream_gene_variant | MODIFIER | c.-1213C>T| |
S230 |
| 90317 | BAA10g00440 | A10 | 211535 | G | A | upstream_gene_variant | MODIFIER | c.-3816C>T| |
S180 |
| 90318 | BAA10g00450 | A10 | 211562 | C | T | missense_variant | MODERATE | c.856G>A|p.Glu286Lys |
S129 |
| 90319 | BAA10g00450 | A10 | 211824 | G | A | synonymous_variant | LOW | c.594C>T|p.Phe198Phe |
S65 |
| 90320 | BAA10g00450 | A10 | 211876 | G | A | missense_variant | MODERATE | c.542C>T|p.Ser181Phe |
S280 |
| 90321 | BAA10g00450 | A10 | 211933 | G | A | missense_variant | MODERATE | c.485C>T|p.Ala162Val |
S18 |
| 90322 | BAA10g00450 | A10 | 212099 | C | T | missense_variant | MODERATE | c.319G>A|p.Asp107Asn |
S159 S243 S298 S299 |
| 90323 | BAA10g00450 | A10 | 212193 | G | A | synonymous_variant | LOW | c.225C>T|p.Ser75Ser |
S164 |
| 90324 | BAA10g00450 | A10 | 212359 | G | A | missense_variant | MODERATE | c.59C>T|p.Ser20Leu |
S293 |
| 90325 | BAA10g00450 | A10 | 213224 | G | A | upstream_gene_variant | MODIFIER | c.-807C>T| |
S39 |