| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 163001 | BAA02g09850 | A02 | 4343120 | C | T | upstream_gene_variant | MODIFIER | c.-665G>A| |
S152 |
| 163002 | BAA02g09850 | A02 | 4343166 | G | A | upstream_gene_variant | MODIFIER | c.-711C>T| |
S11 S96 |
| 163003 | BAA02g09860 | A02 | 4343955 | G | A | missense_variant | MODERATE | c.217G>A|p.Asp73Asn |
S159 S243 |
| 163004 | BAA02g09860 | A02 | 4344098 | C | T | missense_variant | MODERATE | c.278C>T|p.Thr93Ile |
S219 S72 |
| 163005 | BAA02g09850 | A02 | 4344219 | G | A | upstream_gene_variant | MODIFIER | c.-1764C>T| |
S296 |
| 163006 | BAA02g09860 | A02 | 4345234 | G | A | missense_variant | MODERATE | c.706G>A|p.Glu236Lys |
S144 |
| 163007 | BAA02g09850 | A02 | 4345561 | C | T | upstream_gene_variant | MODIFIER | c.-3106G>A| |
S19 |
| 163008 | BAA02g09860 | A02 | 4346674 | G | A | missense_variant | MODERATE | c.1033G>A|p.Glu345Lys |
S140 |
| 163009 | BAA02g09860 | A02 | 4347287 | G | A | missense_variant | MODERATE | c.1465G>A|p.Glu489Lys |
S149 |
| 163010 | BAA02g09850 | A02 | 4347380 | G | A | upstream_gene_variant | MODIFIER | c.-4925C>T| |
S47 |
| 163011 | BAA02g09860 | A02 | 4349299 | C | T | downstream_gene_variant | MODIFIER | c.*1075C>T| |
S305 |
| 163012 | BAA02g09860 | A02 | 4349388 | C | T | downstream_gene_variant | MODIFIER | c.*1164C>T| |
S15 S3 |
| 163013 | BAA02g09880 | A02 | 4350899 | G | A | missense_variant | MODERATE | c.986C>T|p.Ala329Val |
S275 |
| 163014 | BAA02g09860 | A02 | 4351489 | G | A | downstream_gene_variant | MODIFIER | c.*3265G>A| |
S48 |
| 163015 | BAA02g09860 | A02 | 4351542 | G | A | downstream_gene_variant | MODIFIER | c.*3318G>A| |
S197 |
| 163016 | BAA02g09860 | A02 | 4351577 | G | A | downstream_gene_variant | MODIFIER | c.*3353G>A| |
S296 |
| 163017 | BAA02g09860 | A02 | 4351622 | C | T | downstream_gene_variant | MODIFIER | c.*3398C>T| |
S9 |
| 163018 | BAA02g09860 | A02 | 4351715 | G | A | downstream_gene_variant | MODIFIER | c.*3491G>A| |
S165 |
| 163019 | BAA02g09880 | A02 | 4352249 | G | A | missense_variant | MODERATE | c.647C>T|p.Pro216Leu |
S165 |
| 163020 | BAA02g09880 | A02 | 4352544 | C | T | splice_region_variant&synonymous_variant | LOW | c.429G>A|p.Arg143Arg |
S200 |
| 163021 | BAA02g09880 | A02 | 4353387 | G | A | upstream_gene_variant | MODIFIER | c.-251C>T| |
S246 |
| 163022 | BAA02g09880 | A02 | 4353927 | T | C | upstream_gene_variant | MODIFIER | c.-791A>G| |
S97 |
| 163023 | BAA02g09880 | A02 | 4354404 | G | A | upstream_gene_variant | MODIFIER | c.-1268C>T| |
S293 |
| 163024 | BAA02g09880 | A02 | 4354505 | G | A | upstream_gene_variant | MODIFIER | c.-1369C>T| |
S5 |
| 163025 | BAA02g09880 | A02 | 4354525 | G | A | upstream_gene_variant | MODIFIER | c.-1389C>T| |
S217 S248 S52 |