| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 105051 | BAA10g08060-BAA10g08070 | A10 | 5411519 | G | A | intergenic_region | MODIFIER | n.5411519G>A| |
S215 |
| 105052 | BAA10g08060-BAA10g08070 | A10 | 5411567 | G | A | intergenic_region | MODIFIER | n.5411567G>A| |
S57 |
| 105053 | BAA10g08070 | A10 | 5413149 | G | A | downstream_gene_variant | MODIFIER | c.*4699C>T| |
S125 |
| 105054 | BAA10g08070 | A10 | 5413333 | C | T | downstream_gene_variant | MODIFIER | c.*4515G>A| |
S47 |
| 105055 | BAA10g08070 | A10 | 5413387 | G | A | downstream_gene_variant | MODIFIER | c.*4461C>T| |
S172 S217 |
| 105056 | BAA10g08070 | A10 | 5413497 | C | T | downstream_gene_variant | MODIFIER | c.*4351G>A| |
S114 |
| 105057 | BAA10g08070 | A10 | 5413630 | G | A | downstream_gene_variant | MODIFIER | c.*4218C>T| |
S165 |
| 105058 | BAA10g08070 | A10 | 5413833 | G | A | downstream_gene_variant | MODIFIER | c.*4015C>T| |
S16 |
| 105059 | BAA10g08070 | A10 | 5415091 | G | A | downstream_gene_variant | MODIFIER | c.*2757C>T| |
S291 |
| 105060 | BAA10g08070 | A10 | 5415705 | G | A | downstream_gene_variant | MODIFIER | c.*2143C>T| |
S13 |
| 105061 | BAA10g08070 | A10 | 5416031 | G | A | downstream_gene_variant | MODIFIER | c.*1817C>T| |
S274 |
| 105062 | BAA10g08070 | A10 | 5416361 | G | A | downstream_gene_variant | MODIFIER | c.*1487C>T| |
S295 |
| 105063 | BAA10g08070 | A10 | 5416832 | G | A | downstream_gene_variant | MODIFIER | c.*1016C>T| |
S280 |
| 105064 | BAA10g08070 | A10 | 5417080 | G | A | downstream_gene_variant | MODIFIER | c.*768C>T| |
S283 |
| 105065 | BAA10g08070 | A10 | 5417622 | G | A | downstream_gene_variant | MODIFIER | c.*226C>T| |
S1 S90 |
| 105066 | BAA10g08070 | A10 | 5418158 | C | T | missense_variant | MODERATE | c.1700G>A|p.Gly567Glu |
S132 S137 S215 S89 |
| 105067 | BAA10g08070 | A10 | 5418267 | C | T | missense_variant | MODERATE | c.1591G>A|p.Gly531Arg |
S142 |
| 105068 | BAA10g08070 | A10 | 5418325 | C | T | stop_gained | HIGH | c.1533G>A|p.Trp511* |
S11 |
| 105069 | BAA10g08070 | A10 | 5418577 | C | T | synonymous_variant | LOW | c.1281G>A|p.Glu427Glu |
S122 |
| 105070 | BAA10g08070 | A10 | 5418737 | G | A | missense_variant | MODERATE | c.1121C>T|p.Ser374Phe |
S245 |
| 105071 | BAA10g08070 | A10 | 5419296 | G | A | missense_variant | MODERATE | c.562C>T|p.Pro188Ser |
S158 |
| 105072 | BAA10g08070 | A10 | 5419689 | C | T | missense_variant | MODERATE | c.247G>A|p.Glu83Lys |
S12 |
| 105073 | BAA10g08070 | A10 | 5419943 | G | A | upstream_gene_variant | MODIFIER | c.-8C>T| |
S15 S3 |
| 105074 | BAA10g08070 | A10 | 5420033 | C | T | upstream_gene_variant | MODIFIER | c.-98G>A| |
S196 |
| 105075 | BAA10g08070 | A10 | 5420253 | C | T | upstream_gene_variant | MODIFIER | c.-318G>A| |
S6 |