| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 46101 | BAA01g27380-BAA01g27390 | A01 | 15810874 | G | A | intergenic_region | MODIFIER | n.15810874G>A| |
S6 |
| 46102 | BAA01g27380-BAA01g27390 | A01 | 15811214 | C | T | intergenic_region | MODIFIER | n.15811214C>T| |
S150 |
| 46103 | BAA01g27380-BAA01g27390 | A01 | 15811359 | C | T | intergenic_region | MODIFIER | n.15811359C>T| |
S69 |
| 46104 | BAA01g27380-BAA01g27390 | A01 | 15811575 | C | T | intergenic_region | MODIFIER | n.15811575C>T| |
S53 |
| 46105 | BAA01g27380-BAA01g27390 | A01 | 15811824 | G | A | intergenic_region | MODIFIER | n.15811824G>A| |
S225 S73 |
| 46106 | BAA01g27380-BAA01g27390 | A01 | 15812102 | G | A | intergenic_region | MODIFIER | n.15812102G>A| |
S275 S60 |
| 46107 | BAA01g27380-BAA01g27390 | A01 | 15812339 | G | A | intergenic_region | MODIFIER | n.15812339G>A| |
S231 S62 |
| 46108 | BAA01g27380-BAA01g27390 | A01 | 15813706 | C | T | intergenic_region | MODIFIER | n.15813706C>T| |
S296 |
| 46109 | BAA01g27380-BAA01g27390 | A01 | 15813847 | G | A | intergenic_region | MODIFIER | n.15813847G>A| |
S98 |
| 46110 | BAA01g27380-BAA01g27390 | A01 | 15814603 | G | A | intergenic_region | MODIFIER | n.15814603G>A| |
|
| 46111 | BAA01g27390 | A01 | 15816990 | C | T | downstream_gene_variant | MODIFIER | c.*2954G>A| |
S143 |
| 46112 | BAA01g27390 | A01 | 15817791 | C | T | downstream_gene_variant | MODIFIER | c.*2153G>A| |
S295 |
| 46113 | BAA01g27390 | A01 | 15818884 | C | T | downstream_gene_variant | MODIFIER | c.*1060G>A| |
S46 |
| 46114 | BAA01g27390 | A01 | 15818918 | G | A | downstream_gene_variant | MODIFIER | c.*1026C>T| |
S163 |
| 46115 | BAA01g27390 | A01 | 15819764 | C | T | downstream_gene_variant | MODIFIER | c.*180G>A| |
S267 |
| 46116 | BAA01g27390 | A01 | 15819903 | C | T | downstream_gene_variant | MODIFIER | c.*41G>A| |
S150 |
| 46117 | BAA01g27390 | A01 | 15820369 | G | A | stop_gained | HIGH | c.1501C>T|p.Gln501* |
S94 |
| 46118 | BAA01g27390 | A01 | 15820513 | C | T | missense_variant | MODERATE | c.1357G>A|p.Glu453Lys |
S81 S85 |
| 46119 | BAA01g27390 | A01 | 15820955 | C | T | synonymous_variant | LOW | c.915G>A|p.Lys305Lys |
S219 S72 |
| 46120 | BAA01g27390 | A01 | 15821010 | G | A | missense_variant | MODERATE | c.860C>T|p.Ser287Phe |
S84 S93 |
| 46121 | BAA01g27390 | A01 | 15821915 | C | T | intron_variant | MODIFIER | c.120+121G>A| |
S8 |
| 46122 | BAA01g27390 | A01 | 15823433 | G | A | upstream_gene_variant | MODIFIER | c.-983C>T| |
S172 |
| 46123 | BAA01g27390 | A01 | 15823475 | C | T | upstream_gene_variant | MODIFIER | c.-1025G>A| |
S152 |
| 46124 | BAA01g27390 | A01 | 15823915 | G | A | upstream_gene_variant | MODIFIER | c.-1465C>T| |
S266 |
| 46125 | BAA01g27390 | A01 | 15823929 | G | A | upstream_gene_variant | MODIFIER | c.-1479C>T| |
S163 |