| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 42151 | BAA01g26130 | A01 | 14519027 | G | A | upstream_gene_variant | MODIFIER | c.-2181C>T| |
S56 |
| 42152 | BAA01g26130 | A01 | 14519363 | G | A | upstream_gene_variant | MODIFIER | c.-2517C>T| |
S175 |
| 42153 | BAA01g26160 | A01 | 14519435 | G | A | missense_variant | MODERATE | c.23G>A|p.Ser8Asn |
S103 |
| 42154 | BAA01g26160 | A01 | 14519957 | G | A | missense_variant | MODERATE | c.545G>A|p.Cys182Tyr |
S87 |
| 42155 | BAA01g26130 | A01 | 14520147 | C | T | upstream_gene_variant | MODIFIER | c.-3301G>A| |
S112 |
| 42156 | BAA01g26130 | A01 | 14520227 | G | A | upstream_gene_variant | MODIFIER | c.-3381C>T| |
S293 |
| 42157 | BAA01g26170 | A01 | 14520416 | G | A | missense_variant | MODERATE | c.755C>T|p.Thr252Ile |
S15 S3 |
| 42158 | BAA01g26130 | A01 | 14521094 | C | T | upstream_gene_variant | MODIFIER | c.-4248G>A| |
S146 |
| 42159 | BAA01g26130 | A01 | 14521210 | G | A | upstream_gene_variant | MODIFIER | c.-4364C>T| |
S144 |
| 42160 | BAA01g26130 | A01 | 14521710 | G | A | upstream_gene_variant | MODIFIER | c.-4864C>T| |
S287 |
| 42161 | BAA01g26130 | A01 | 14521811 | G | A | upstream_gene_variant | MODIFIER | c.-4965C>T| |
S86 |
| 42162 | BAA01g26170 | A01 | 14522484 | G | A | missense_variant | MODERATE | c.16C>T|p.Leu6Phe |
S87 |
| 42163 | BAA01g26170 | A01 | 14522535 | C | T | upstream_gene_variant | MODIFIER | c.-36G>A| |
S176 |
| 42164 | BAA01g26170 | A01 | 14522596 | C | T | upstream_gene_variant | MODIFIER | c.-97G>A| |
S177 |
| 42165 | BAA01g26170 | A01 | 14523451 | C | T | upstream_gene_variant | MODIFIER | c.-952G>A| |
S275 |
| 42166 | BAA01g26170 | A01 | 14523973 | C | T | upstream_gene_variant | MODIFIER | c.-1474G>A| |
S104 S52 |
| 42167 | BAA01g26170 | A01 | 14524051 | C | T | upstream_gene_variant | MODIFIER | c.-1552G>A| |
S159 S243 |
| 42168 | BAA01g26180 | A01 | 14524498 | C | T | missense_variant | MODERATE | c.625G>A|p.Gly209Arg |
S41 |
| 42169 | BAA01g26170 | A01 | 14524660 | C | T | upstream_gene_variant | MODIFIER | c.-2161G>A| |
S255 |
| 42170 | BAA01g26170 | A01 | 14525647 | G | A | upstream_gene_variant | MODIFIER | c.-3148C>T| |
S207 |
| 42171 | BAA01g26190 | A01 | 14533267 | C | T | intron_variant | MODIFIER | c.2068-53G>A| |
S17 |
| 42172 | BAA01g26190 | A01 | 14533723 | C | T | intron_variant | MODIFIER | c.1816-33G>A| |
S277 |
| 42173 | BAA01g26190 | A01 | 14534210 | C | T | synonymous_variant | LOW | c.1368G>A|p.Leu456Leu |
S260 |
| 42174 | BAA01g26190 | A01 | 14534368 | G | A | stop_gained | HIGH | c.1210C>T|p.Arg404* |
S275 |
| 42175 | BAA01g26190 | A01 | 14535139 | C | T | synonymous_variant | LOW | c.552G>A|p.Arg184Arg |
S273 |