| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 102251 | BAA10g07450 | A10 | 4325599 | G | A | upstream_gene_variant | MODIFIER | c.-3603C>T| |
S274 |
| 102252 | BAA10g07450 | A10 | 4325898 | C | T | upstream_gene_variant | MODIFIER | c.-3902G>A| |
S176 |
| 102253 | BAA10g07470 | A10 | 4332685 | G | A | splice_region_variant&intron_variant | LOW | c.609+8C>T| |
S255 |
| 102254 | BAA10g07460 | A10 | 4333765 | C | T | downstream_gene_variant | MODIFIER | c.*3886C>T| |
S143 |
| 102255 | BAA10g07470 | A10 | 4334150 | C | T | synonymous_variant | LOW | c.207G>A|p.Glu69Glu |
S305 |
| 102256 | BAA10g07470 | A10 | 4334264 | G | A | splice_region_variant&intron_variant | LOW | c.98-5C>T| |
S33 |
| 102257 | BAA10g07480 | A10 | 4337637 | C | T | upstream_gene_variant | MODIFIER | c.-4385C>T| |
S259 |
| 102258 | BAA10g07480 | A10 | 4338044 | G | A | upstream_gene_variant | MODIFIER | c.-3978G>A| |
S268 |
| 102259 | BAA10g07480 | A10 | 4338305 | C | T | upstream_gene_variant | MODIFIER | c.-3717C>T| |
S288 |
| 102260 | BAA10g07480 | A10 | 4338761 | G | A | upstream_gene_variant | MODIFIER | c.-3261G>A| |
S136 |
| 102261 | BAA10g07480 | A10 | 4338858 | C | T | upstream_gene_variant | MODIFIER | c.-3164C>T| |
S125 |
| 102262 | BAA10g07480 | A10 | 4340035 | G | A | upstream_gene_variant | MODIFIER | c.-1987G>A| |
S128 |
| 102263 | BAA10g07480 | A10 | 4341121 | G | A | upstream_gene_variant | MODIFIER | c.-901G>A| |
S135 S273 S68 |
| 102264 | BAA10g07480 | A10 | 4341198 | C | T | upstream_gene_variant | MODIFIER | c.-824C>T| |
S40 S49 |
| 102265 | BAA10g07480 | A10 | 4341504 | G | A | upstream_gene_variant | MODIFIER | c.-518G>A| |
S59 |
| 102266 | BAA10g07480 | A10 | 4342422 | C | T | synonymous_variant | LOW | c.219C>T|p.Phe73Phe |
S117 |
| 102267 | BAA10g07480 | A10 | 4342868 | G | A | missense_variant | MODERATE | c.628G>A|p.Ala210Thr |
S53 |
| 102268 | BAA10g07470 | A10 | 4343279 | A | T | upstream_gene_variant | MODIFIER | c.-1425T>A| |
S132 S160 S183 S294 S297 S3 S308 S48 |
| 102269 | BAA10g07480 | A10 | 4343639 | C | T | missense_variant | MODERATE | c.904C>T|p.Arg302Cys |
S41 |
| 102270 | BAA10g07480 | A10 | 4344232 | G | A | missense_variant | MODERATE | c.1339G>A|p.Asp447Asn |
S262 |
| 102271 | BAA10g07480 | A10 | 4344283 | C | T | missense_variant | MODERATE | c.1390C>T|p.Leu464Phe |
S61 |
| 102272 | BAA10g07480 | A10 | 4344535 | G | A | missense_variant | MODERATE | c.1642G>A|p.Asp548Asn |
S125 |
| 102273 | BAA10g07470 | A10 | 4345799 | G | A | upstream_gene_variant | MODIFIER | c.-3945C>T| |
S274 |
| 102274 | BAA10g07470 | A10 | 4346148 | G | A | upstream_gene_variant | MODIFIER | c.-4294C>T| |
S13 |
| 102275 | BAA10g07470 | A10 | 4346425 | G | A | upstream_gene_variant | MODIFIER | c.-4571C>T| |
S262 |