| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 52101 | BAA01g28740 | A01 | 18056795 | C | T | upstream_gene_variant | MODIFIER | c.-196G>A| |
S240 |
| 52102 | BAA01g28740 | A01 | 18056972 | C | T | upstream_gene_variant | MODIFIER | c.-373G>A| |
S291 |
| 52103 | BAA01g28740 | A01 | 18057073 | C | T | upstream_gene_variant | MODIFIER | c.-474G>A| |
S113 S295 |
| 52104 | BAA01g28740 | A01 | 18057174 | G | A | upstream_gene_variant | MODIFIER | c.-575C>T| |
S151 |
| 52105 | BAA01g28740 | A01 | 18057519 | C | T | upstream_gene_variant | MODIFIER | c.-920G>A| |
S303 |
| 52106 | BAA01g28740 | A01 | 18057758 | G | A | upstream_gene_variant | MODIFIER | c.-1159C>T| |
S221 |
| 52107 | BAA01g28750 | A01 | 18059861 | C | T | missense_variant | MODERATE | c.1028C>T|p.Ser343Phe |
S233 |
| 52108 | BAA01g28740 | A01 | 18060042 | G | A | upstream_gene_variant | MODIFIER | c.-3443C>T| |
S181 |
| 52109 | BAA01g28740 | A01 | 18060090 | C | T | upstream_gene_variant | MODIFIER | c.-3491G>A| |
S205 |
| 52110 | BAA01g28740 | A01 | 18060449 | G | A | upstream_gene_variant | MODIFIER | c.-3850C>T| |
S74 |
| 52111 | BAA01g28740 | A01 | 18061022 | G | A | upstream_gene_variant | MODIFIER | c.-4423C>T| |
S257 |
| 52112 | BAA01g28750 | A01 | 18062895 | C | T | downstream_gene_variant | MODIFIER | c.*2985C>T| |
S128 |
| 52113 | BAA01g28750 | A01 | 18063218 | C | T | downstream_gene_variant | MODIFIER | c.*3308C>T| |
S198 |
| 52114 | BAA01g28750 | A01 | 18063871 | G | A | downstream_gene_variant | MODIFIER | c.*3961G>A| |
S305 |
| 52115 | BAA01g28760 | A01 | 18065058 | C | T | downstream_gene_variant | MODIFIER | c.*3262G>A| |
S150 |
| 52116 | BAA01g28760 | A01 | 18065185 | C | T | downstream_gene_variant | MODIFIER | c.*3135G>A| |
S261 |
| 52117 | BAA01g28760 | A01 | 18065528 | C | T | downstream_gene_variant | MODIFIER | c.*2792G>A| |
S231 |
| 52118 | BAA01g28760 | A01 | 18066813 | C | T | downstream_gene_variant | MODIFIER | c.*1507G>A| |
S148 S210 |
| 52119 | BAA01g28760 | A01 | 18067037 | C | T | downstream_gene_variant | MODIFIER | c.*1283G>A| |
S130 |
| 52120 | BAA01g28760 | A01 | 18067269 | C | T | downstream_gene_variant | MODIFIER | c.*1051G>A| |
S286 |
| 52121 | BAA01g28760 | A01 | 18070359 | A | G | missense_variant | MODERATE | c.518T>C|p.Met173Thr |
S104 S105 S52 |
| 52122 | BAA01g28760 | A01 | 18072208 | C | T | upstream_gene_variant | MODIFIER | c.-1267G>A| |
S198 |
| 52123 | BAA01g28760 | A01 | 18072669 | C | T | upstream_gene_variant | MODIFIER | c.-1728G>A| |
S139 |
| 52124 | BAA01g28770 | A01 | 18075167 | C | T | missense_variant | MODERATE | c.1423C>T|p.Pro475Ser |
S271 |
| 52125 | BAA01g28770 | A01 | 18075191 | G | A | missense_variant | MODERATE | c.1447G>A|p.Asp483Asn |
S218 |