| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 67951 | BAA01g35630-BAA01g35640 | A01 | 23835064 | G | A | intergenic_region | MODIFIER | n.23835064G>A| |
S172 S217 |
| 67952 | BAA01g35630-BAA01g35640 | A01 | 23835130 | G | A | intergenic_region | MODIFIER | n.23835130G>A| |
S173 |
| 67953 | BAA01g35630-BAA01g35640 | A01 | 23835706 | G | A | intergenic_region | MODIFIER | n.23835706G>A| |
S99 |
| 67954 | BAA01g35640 | A01 | 23836417 | C | T | upstream_gene_variant | MODIFIER | c.-4772C>T| |
S128 |
| 67955 | BAA01g35640 | A01 | 23836849 | G | A | upstream_gene_variant | MODIFIER | c.-4340G>A| |
S6 |
| 67956 | BAA01g35640 | A01 | 23836898 | G | A | upstream_gene_variant | MODIFIER | c.-4291G>A| |
S225 |
| 67957 | BAA01g35640 | A01 | 23837390 | G | A | upstream_gene_variant | MODIFIER | c.-3799G>A| |
S135 |
| 67958 | BAA01g35640 | A01 | 23839083 | C | T | upstream_gene_variant | MODIFIER | c.-2106C>T| |
S46 |
| 67959 | BAA01g35640 | A01 | 23840924 | G | A | upstream_gene_variant | MODIFIER | c.-265G>A| |
S79 S91 |
| 67960 | BAA01g35640 | A01 | 23841083 | C | T | upstream_gene_variant | MODIFIER | c.-106C>T| |
S166 |
| 67961 | BAA01g35640 | A01 | 23841527 | C | T | synonymous_variant | LOW | c.339C>T|p.His113His |
S167 |
| 67962 | BAA01g35640 | A01 | 23841648 | C | T | synonymous_variant | LOW | c.460C>T|p.Leu154Leu |
S243 |
| 67963 | BAA01g35640 | A01 | 23841697 | G | A | missense_variant | MODERATE | c.509G>A|p.Arg170Lys |
S86 |
| 67964 | BAA01g35640 | A01 | 23842197 | G | A | missense_variant | MODERATE | c.797G>A|p.Cys266Tyr |
S155 |
| 67965 | BAA01g35640 | A01 | 23842840 | C | T | synonymous_variant | LOW | c.1275C>T|p.Asp425Asp |
S153 |
| 67966 | BAA01g35640 | A01 | 23843289 | G | A | missense_variant | MODERATE | c.1640G>A|p.Gly547Glu |
S125 |
| 67967 | BAA01g35650 | A01 | 23844469 | G | A | upstream_gene_variant | MODIFIER | c.-23G>A| |
S291 |
| 67968 | BAA01g35650 | A01 | 23844625 | C | T | missense_variant | MODERATE | c.134C>T|p.Thr45Ile |
S18 |
| 67969 | BAA01g35660 | A01 | 23844843 | C | T | upstream_gene_variant | MODIFIER | c.-1450C>T| |
S153 |
| 67970 | BAA01g35660 | A01 | 23845935 | C | T | upstream_gene_variant | MODIFIER | c.-358C>T| |
S293 |
| 67971 | BAA01g35660 | A01 | 23847619 | C | T | missense_variant | MODERATE | c.599C>T|p.Ser200Phe |
S48 |
| 67972 | BAA01g35660 | A01 | 23847888 | C | T | missense_variant | MODERATE | c.785C>T|p.Ser262Phe |
S150 |
| 67973 | BAA01g35640 | A01 | 23848684 | C | T | downstream_gene_variant | MODIFIER | c.*4711C>T| |
S295 |
| 67974 | BAA01g35640 | A01 | 23848856 | C | T | downstream_gene_variant | MODIFIER | c.*4883C>T| |
S233 |
| 67975 | BAA01g35650 | A01 | 23849009 | C | T | downstream_gene_variant | MODIFIER | c.*4197C>T| |
S216 |