| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 97851 | BAA10g05630 | A10 | 2892202 | C | T | upstream_gene_variant | MODIFIER | c.-673G>A| |
S146 |
| 97852 | BAA10g05640 | A10 | 2892413 | C | T | synonymous_variant | LOW | c.243G>A|p.Leu81Leu |
S176 |
| 97853 | BAA10g05640 | A10 | 2892432 | G | A | missense_variant | MODERATE | c.224C>T|p.Ser75Phe |
S25 |
| 97854 | BAA10g05640 | A10 | 2892550 | G | A | synonymous_variant | LOW | c.106C>T|p.Leu36Leu |
S209 |
| 97855 | BAA10g05630 | A10 | 2892750 | G | A | upstream_gene_variant | MODIFIER | c.-1221C>T| |
S128 |
| 97856 | BAA10g05630 | A10 | 2892838 | G | A | upstream_gene_variant | MODIFIER | c.-1309C>T| |
S134 |
| 97857 | BAA10g05630 | A10 | 2892968 | G | A | upstream_gene_variant | MODIFIER | c.-1439C>T| |
S178 |
| 97858 | BAA10g05630 | A10 | 2893300 | G | A | upstream_gene_variant | MODIFIER | c.-1771C>T| |
S198 |
| 97859 | BAA10g05630 | A10 | 2893721 | G | A | upstream_gene_variant | MODIFIER | c.-2192C>T| |
S291 |
| 97860 | BAA10g05630 | A10 | 2894336 | G | A | upstream_gene_variant | MODIFIER | c.-2807C>T| |
S179 |
| 97861 | BAA10g05630 | A10 | 2894402 | G | A | upstream_gene_variant | MODIFIER | c.-2873C>T| |
S268 |
| 97862 | BAA10g05630 | A10 | 2894865 | C | T | upstream_gene_variant | MODIFIER | c.-3336G>A| |
S282 |
| 97863 | BAA10g05630 | A10 | 2895570 | C | T | upstream_gene_variant | MODIFIER | c.-4041G>A| |
S2 |
| 97864 | BAA10g05640 | A10 | 2896761 | G | A | upstream_gene_variant | MODIFIER | c.-4106C>T| |
S153 S213 |
| 97865 | BAA10g05640 | A10 | 2896812 | G | A | upstream_gene_variant | MODIFIER | c.-4157C>T| |
S208 |
| 97866 | BAA10g05660 | A10 | 2897542 | G | A | missense_variant | MODERATE | c.2408C>T|p.Thr803Ile |
S138 |
| 97867 | BAA10g05660 | A10 | 2899741 | C | T | synonymous_variant | LOW | c.1200G>A|p.Gln400Gln |
S119 |
| 97868 | BAA10g05650 | A10 | 2900886 | G | A | downstream_gene_variant | MODIFIER | c.*4854G>A| |
S115 |
| 97869 | BAA10g05660 | A10 | 2901075 | C | T | intron_variant | MODIFIER | c.755+62G>A| |
S205 |
| 97870 | BAA10g05660 | A10 | 2902163 | C | T | intron_variant | MODIFIER | c.248+59G>A| |
S2 |
| 97871 | BAA10g05660 | A10 | 2903853 | G | A | upstream_gene_variant | MODIFIER | c.-1283C>T| |
S296 |
| 97872 | BAA10g05660 | A10 | 2904250 | G | A | upstream_gene_variant | MODIFIER | c.-1680C>T| |
S179 |
| 97873 | BAA10g05660 | A10 | 2904713 | G | A | upstream_gene_variant | MODIFIER | c.-2143C>T| |
S230 |
| 97874 | BAA10g05660 | A10 | 2904807 | C | T | upstream_gene_variant | MODIFIER | c.-2237G>A| |
S143 |
| 97875 | BAA10g05660 | A10 | 2905350 | C | T | upstream_gene_variant | MODIFIER | c.-2780G>A| |
S68 |