| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 134051 | BAA10g20330 | A10 | 18341951 | G | A | missense_variant | MODERATE | c.4864G>A|p.Ala1622Thr |
S18 |
| 134052 | BAA10g20340 | A10 | 18342560 | G | A | missense_variant | MODERATE | c.1135C>T|p.Leu379Phe |
S105 S106 |
| 134053 | BAA10g20340 | A10 | 18342623 | C | T | missense_variant | MODERATE | c.1072G>A|p.Asp358Asn |
S297 |
| 134054 | BAA10g20340 | A10 | 18342885 | G | A | synonymous_variant | LOW | c.810C>T|p.Ala270Ala |
S265 |
| 134055 | BAA10g20340 | A10 | 18344076 | G | A | upstream_gene_variant | MODIFIER | c.-149C>T| |
S191 |
| 134056 | BAA10g20340 | A10 | 18344307 | G | A | upstream_gene_variant | MODIFIER | c.-380C>T| |
S136 |
| 134057 | BAA10g20340 | A10 | 18344432 | G | A | upstream_gene_variant | MODIFIER | c.-505C>T| |
S28 |
| 134058 | BAA10g20340 | A10 | 18344510 | C | T | upstream_gene_variant | MODIFIER | c.-583G>A| |
S281 |
| 134059 | BAA10g20350 | A10 | 18345972 | G | A | synonymous_variant | LOW | c.603G>A|p.Thr201Thr |
S284 |
| 134060 | BAA10g20350 | A10 | 18346921 | C | T | missense_variant | MODERATE | c.1552C>T|p.Pro518Ser |
S23 |
| 134061 | BAA10g20350 | A10 | 18347372 | G | A | missense_variant | MODERATE | c.2003G>A|p.Gly668Asp |
S303 |
| 134062 | BAA10g20340 | A10 | 18348693 | C | T | upstream_gene_variant | MODIFIER | c.-4766G>A| |
S150 |
| 134063 | BAA10g20360 | A10 | 18348950 | C | T | synonymous_variant | LOW | c.183C>T|p.Leu61Leu |
S146 |
| 134064 | BAA10g20360 | A10 | 18349600 | G | A | synonymous_variant | LOW | c.660G>A|p.Lys220Lys |
S250 |
| 134065 | BAA10g20370 | A10 | 18349850 | G | A | upstream_gene_variant | MODIFIER | c.-1030G>A| |
S184 |
| 134066 | BAA10g20370 | A10 | 18350199 | C | T | upstream_gene_variant | MODIFIER | c.-681C>T| |
S84 S93 |
| 134067 | BAA10g20370 | A10 | 18351165 | G | A | missense_variant | MODERATE | c.208G>A|p.Glu70Lys |
S9 |
| 134068 | BAA10g20350 | A10 | 18351409 | C | T | downstream_gene_variant | MODIFIER | c.*3694C>T| |
S168 S219 S72 |
| 134069 | BAA10g20350 | A10 | 18351421 | G | A | downstream_gene_variant | MODIFIER | c.*3706G>A| |
S57 |
| 134070 | BAA10g20370 | A10 | 18352932 | G | A | missense_variant | MODERATE | c.1232G>A|p.Arg411Gln |
S288 |
| 134071 | BAA10g20360 | A10 | 18353302 | G | A | downstream_gene_variant | MODIFIER | c.*3678G>A| |
S211 S227 |
| 134072 | BAA10g20370 | A10 | 18353377 | G | A | missense_variant | MODERATE | c.1291G>A|p.Glu431Lys |
S178 |
| 134073 | BAA10g20370 | A10 | 18353379 | G | A | synonymous_variant | LOW | c.1293G>A|p.Glu431Glu |
S138 |
| 134074 | BAA10g20370 | A10 | 18353431 | G | A | missense_variant | MODERATE | c.1345G>A|p.Glu449Lys |
S62 |
| 134075 | BAA10g20370 | A10 | 18353649 | G | A | missense_variant | MODERATE | c.1435G>A|p.Ala479Thr |
S155 S211 |