| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 123101 | BAA10g13140 | A10 | 14384881 | C | T | upstream_gene_variant | MODIFIER | c.-2680C>T| |
S281 |
| 123102 | BAA10g13140 | A10 | 14384983 | G | A | upstream_gene_variant | MODIFIER | c.-2578G>A| |
S278 |
| 123103 | BAA10g13140 | A10 | 14385436 | C | T | upstream_gene_variant | MODIFIER | c.-2125C>T| |
S96 |
| 123104 | BAA10g13140 | A10 | 14386100 | G | A | upstream_gene_variant | MODIFIER | c.-1461G>A| |
S72 |
| 123105 | BAA10g13140 | A10 | 14387009 | C | T | upstream_gene_variant | MODIFIER | c.-552C>T| |
S302 |
| 123106 | BAA10g13140 | A10 | 14387597 | C | T | synonymous_variant | LOW | c.37C>T|p.Leu13Leu |
S86 |
| 123107 | BAA10g13140 | A10 | 14387743 | C | T | synonymous_variant | LOW | c.183C>T|p.Val61Val |
S246 |
| 123108 | BAA10g13140 | A10 | 14388003 | G | A | downstream_gene_variant | MODIFIER | c.*110G>A| |
S287 |
| 123109 | BAA10g13150 | A10 | 14389669 | G | A | synonymous_variant | LOW | c.834C>T|p.Phe278Phe |
S226 |
| 123110 | BAA10g13150 | A10 | 14389688 | C | T | missense_variant | MODERATE | c.815G>A|p.Gly272Glu |
S42 |
| 123111 | BAA10g13150 | A10 | 14389702 | G | A | splice_region_variant&synonymous_variant | LOW | c.801C>T|p.Leu267Leu |
S198 |
| 123112 | BAA10g13150 | A10 | 14391927 | G | A | upstream_gene_variant | MODIFIER | c.-686C>T| |
S68 |
| 123113 | BAA10g13150 | A10 | 14392033 | C | T | upstream_gene_variant | MODIFIER | c.-792G>A| |
S256 |
| 123114 | BAA10g13150 | A10 | 14392066 | G | A | upstream_gene_variant | MODIFIER | c.-825C>T| |
S192 |
| 123115 | BAA10g13150 | A10 | 14392440 | G | A | upstream_gene_variant | MODIFIER | c.-1199C>T| |
S184 |
| 123116 | BAA10g13150 | A10 | 14393270 | G | A | upstream_gene_variant | MODIFIER | c.-2029C>T| |
S13 S140 S219 S279 S72 |
| 123117 | BAA10g13150 | A10 | 14393851 | G | A | upstream_gene_variant | MODIFIER | c.-2610C>T| |
S105 S106 |
| 123118 | BAA10g13160 | A10 | 14395750 | G | A | splice_region_variant&intron_variant | LOW | c.143-8G>A| |
S169 |
| 123119 | BAA10g13160 | A10 | 14395767 | C | T | missense_variant | MODERATE | c.152C>T|p.Pro51Leu |
S199 |
| 123120 | BAA10g13160 | A10 | 14397489 | C | T | missense_variant | MODERATE | c.797C>T|p.Ala266Val |
S275 |
| 123121 | BAA10g13160 | A10 | 14398086 | C | T | missense_variant | MODERATE | c.1241C>T|p.Ser414Leu |
S180 |
| 123122 | BAA10g13160 | A10 | 14398850 | C | T | synonymous_variant | LOW | c.1716C>T|p.Ile572Ile |
S165 |
| 123123 | BAA10g13160 | A10 | 14399024 | G | A | synonymous_variant | LOW | c.1890G>A|p.Glu630Glu |
S112 |
| 123124 | BAA10g13170 | A10 | 14401447 | C | T | missense_variant | MODERATE | c.772G>A|p.Gly258Arg |
S229 |
| 123125 | BAA10g13170 | A10 | 14402177 | G | A | missense_variant | MODERATE | c.116C>T|p.Ser39Phe |
S264 |