| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 116001 | BAA10g10090 | A10 | 11859796 | C | T | upstream_gene_variant | MODIFIER | c.-4700C>T| |
S203 |
| 116002 | BAA10g10090 | A10 | 11860462 | G | A | upstream_gene_variant | MODIFIER | c.-4034G>A| |
S132 S137 S215 S89 |
| 116003 | BAA10g10090 | A10 | 11862233 | G | A | upstream_gene_variant | MODIFIER | c.-2263G>A| |
S245 |
| 116004 | BAA10g10090 | A10 | 11863218 | G | A | upstream_gene_variant | MODIFIER | c.-1278G>A| |
S296 |
| 116005 | BAA10g10090 | A10 | 11863321 | C | T | upstream_gene_variant | MODIFIER | c.-1175C>T| |
S44 |
| 116006 | BAA10g10090 | A10 | 11863482 | G | A | upstream_gene_variant | MODIFIER | c.-1014G>A| |
S71 |
| 116007 | BAA10g10090 | A10 | 11863635 | G | A | upstream_gene_variant | MODIFIER | c.-861G>A| |
S125 |
| 116008 | BAA10g10090 | A10 | 11864439 | C | T | upstream_gene_variant | MODIFIER | c.-57C>T| |
S124 |
| 116009 | BAA10g10110 | A10 | 11864917 | G | A | upstream_gene_variant | MODIFIER | c.-2804G>A| |
S303 |
| 116010 | BAA10g10100 | A10 | 11866347 | G | A | synonymous_variant | LOW | c.234C>T|p.Ile78Ile |
S158 |
| 116011 | BAA10g10100 | A10 | 11866352 | C | T | missense_variant | MODERATE | c.229G>A|p.Glu77Lys |
S246 |
| 116012 | BAA10g10110 | A10 | 11866522 | G | A | upstream_gene_variant | MODIFIER | c.-1199G>A| |
S273 |
| 116013 | BAA10g10100 | A10 | 11866559 | G | A | synonymous_variant | LOW | c.135C>T|p.Ile45Ile |
S151 S263 |
| 116014 | BAA10g10100 | A10 | 11867279 | G | A | upstream_gene_variant | MODIFIER | c.-586C>T| |
S71 |
| 116015 | BAA10g10100 | A10 | 11867340 | G | A | upstream_gene_variant | MODIFIER | c.-647C>T| |
S245 |
| 116016 | BAA10g10100 | A10 | 11867430 | C | T | upstream_gene_variant | MODIFIER | c.-737G>A| |
S61 |
| 116017 | BAA10g10100 | A10 | 11868711 | G | A | upstream_gene_variant | MODIFIER | c.-2018C>T| |
S179 |
| 116018 | BAA10g10100 | A10 | 11868765 | C | T | upstream_gene_variant | MODIFIER | c.-2072G>A| |
S269 |
| 116019 | BAA10g10100 | A10 | 11869544 | C | T | upstream_gene_variant | MODIFIER | c.-2851G>A| |
S42 |
| 116020 | BAA10g10100 | A10 | 11871125 | C | T | upstream_gene_variant | MODIFIER | c.-4432G>A| |
S23 |
| 116021 | BAA10g10120 | A10 | 11871568 | C | T | missense_variant | MODERATE | c.1243C>T|p.Leu415Phe |
S84 S93 |
| 116022 | BAA10g10110 | A10 | 11871711 | C | T | downstream_gene_variant | MODIFIER | c.*3301C>T| |
S116 |
| 116023 | BAA10g10110 | A10 | 11872135 | C | T | downstream_gene_variant | MODIFIER | c.*3725C>T| |
S260 |
| 116024 | BAA10g10130 | A10 | 11878787 | C | T | upstream_gene_variant | MODIFIER | c.-533C>T| |
S259 |
| 116025 | BAA10g10130 | A10 | 11878843 | C | T | upstream_gene_variant | MODIFIER | c.-477C>T| |
S56 |