| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 118151 | BAA10g10870 | A10 | 12623772 | C | T | upstream_gene_variant | MODIFIER | c.-4793G>A| |
S123 |
| 118152 | BAA10g10870 | A10 | 12623911 | G | A | upstream_gene_variant | MODIFIER | c.-4932C>T| |
S67 |
| 118153 | BAA10g10880 | A10 | 12624630 | C | T | upstream_gene_variant | MODIFIER | c.-28C>T| |
S247 |
| 118154 | BAA10g10880 | A10 | 12624743 | C | T | missense_variant | MODERATE | c.86C>T|p.Pro29Leu |
S157 |
| 118155 | BAA10g10880 | A10 | 12624979 | C | T | intron_variant | MODIFIER | c.242+80C>T| |
S78 |
| 118156 | BAA10g10880 | A10 | 12625367 | C | T | missense_variant | MODERATE | c.329C>T|p.Ser110Phe |
S17 |
| 118157 | BAA10g10880 | A10 | 12625739 | G | A | intron_variant | MODIFIER | c.374-49G>A| |
S279 |
| 118158 | BAA10g10880 | A10 | 12625846 | C | T | synonymous_variant | LOW | c.432C>T|p.Asn144Asn |
S34 |
| 118159 | BAA10g10880 | A10 | 12625868 | C | T | missense_variant | MODERATE | c.454C>T|p.Pro152Ser |
S282 |
| 118160 | BAA10g10880 | A10 | 12626312 | C | T | intron_variant | MODIFIER | c.550-194C>T| |
S256 |
| 118161 | BAA10g10880 | A10 | 12626396 | C | T | intron_variant | MODIFIER | c.550-110C>T| |
S133 |
| 118162 | BAA10g10880 | A10 | 12626405 | C | T | intron_variant | MODIFIER | c.550-101C>T| |
S135 |
| 118163 | BAA10g10880 | A10 | 12626753 | G | A | splice_region_variant&intron_variant | LOW | c.719+6G>A| |
S112 |
| 118164 | BAA10g10880 | A10 | 12626892 | G | A | splice_region_variant&synonymous_variant | LOW | c.720G>A|p.Arg240Arg |
S303 |
| 118165 | BAA10g10880 | A10 | 12627501 | G | A | downstream_gene_variant | MODIFIER | c.*369G>A| |
S289 |
| 118166 | BAA10g10880 | A10 | 12629829 | G | A | downstream_gene_variant | MODIFIER | c.*2697G>A| |
S295 |
| 118167 | BAA10g10880 | A10 | 12629854 | G | A | downstream_gene_variant | MODIFIER | c.*2722G>A| |
S192 |
| 118168 | BAA10g10880 | A10 | 12629889 | G | A | downstream_gene_variant | MODIFIER | c.*2757G>A| |
S202 |
| 118169 | BAA10g10880 | A10 | 12630207 | G | A | downstream_gene_variant | MODIFIER | c.*3075G>A| |
S234 |
| 118170 | BAA10g10880 | A10 | 12630341 | C | T | downstream_gene_variant | MODIFIER | c.*3209C>T| |
S117 |
| 118171 | BAA10g10880 | A10 | 12630359 | G | A | downstream_gene_variant | MODIFIER | c.*3227G>A| |
S207 |
| 118172 | BAA10g10880 | A10 | 12631883 | G | A | downstream_gene_variant | MODIFIER | c.*4751G>A| |
S245 |
| 118173 | BAA10g10890 | A10 | 12632301 | T | A | downstream_gene_variant | MODIFIER | c.*2507A>T| |
S275 |
| 118174 | BAA10g10890 | A10 | 12633437 | G | A | downstream_gene_variant | MODIFIER | c.*1371C>T| |
S15 S3 |
| 118175 | BAA10g10890 | A10 | 12633834 | T | A | downstream_gene_variant | MODIFIER | c.*974A>T| |
S197 S210 S220 S225 S229 |