| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 90101 | BAA10g00220 | A10 | 98499 | C | T | missense_variant | MODERATE | c.2350G>A|p.Glu784Lys |
S266 |
| 90102 | BAA10g00220 | A10 | 98750 | C | T | splice_region_variant&intron_variant | LOW | c.2194-8G>A| |
S142 |
| 90103 | BAA10g00220 | A10 | 99578 | C | T | synonymous_variant | LOW | c.1854G>A|p.Leu618Leu |
S184 |
| 90104 | BAA10g00220 | A10 | 100192 | C | T | missense_variant | MODERATE | c.1567G>A|p.Glu523Lys |
S146 |
| 90105 | BAA10g00220 | A10 | 100332 | C | T | synonymous_variant | LOW | c.1509G>A|p.Gln503Gln |
S15 S2 S4 S6 |
| 90106 | BAA10g00220 | A10 | 100356 | C | T | synonymous_variant | LOW | c.1485G>A|p.Lys495Lys |
S294 |
| 90107 | BAA10g00220 | A10 | 100410 | C | T | synonymous_variant | LOW | c.1431G>A|p.Leu477Leu |
S173 |
| 90108 | BAA10g00220 | A10 | 100949 | C | T | missense_variant | MODERATE | c.995G>A|p.Arg332Lys |
S105 S106 |
| 90109 | BAA10g00220 | A10 | 102974 | G | A | upstream_gene_variant | MODIFIER | c.-1031C>T| |
S128 |
| 90110 | BAA10g00230 | A10 | 105519 | C | T | missense_variant | MODERATE | c.3085G>A|p.Gly1029Arg |
S56 |
| 90111 | BAA10g00230 | A10 | 105526 | G | A | synonymous_variant | LOW | c.3078C>T|p.Asp1026Asp |
S262 |
| 90112 | BAA10g00230 | A10 | 106816 | G | A | synonymous_variant | LOW | c.2464C>T|p.Leu822Leu |
S50 |
| 90113 | BAA10g00230 | A10 | 107087 | G | A | stop_gained | HIGH | c.2287C>T|p.Arg763* |
S39 |
| 90114 | BAA10g00240 | A10 | 108129 | G | A | downstream_gene_variant | MODIFIER | c.*3118C>T| |
S32 |
| 90115 | BAA10g00230 | A10 | 109425 | G | A | missense_variant | MODERATE | c.886C>T|p.Arg296Cys |
S83 S88 |
| 90116 | BAA10g00230 | A10 | 109659 | C | T | missense_variant | MODERATE | c.652G>A|p.Glu218Lys |
S67 |
| 90117 | BAA10g00230 | A10 | 110061 | C | T | missense_variant | MODERATE | c.250G>A|p.Glu84Lys |
S283 |
| 90118 | BAA10g00230 | A10 | 110388 | G | A | upstream_gene_variant | MODIFIER | c.-78C>T| |
S38 |
| 90119 | BAA10g00230 | A10 | 110448 | G | A | upstream_gene_variant | MODIFIER | c.-138C>T| |
S166 |
| 90120 | BAA10g00240 | A10 | 112052 | C | T | missense_variant | MODERATE | c.161G>A|p.Gly54Glu |
S273 |
| 90121 | BAA10g00240 | A10 | 112303 | G | A | missense_variant | MODERATE | c.86C>T|p.Pro29Leu |
S4 |
| 90122 | BAA10g00230 | A10 | 114032 | C | T | upstream_gene_variant | MODIFIER | c.-3722G>A| |
S143 |
| 90123 | BAA10g00230 | A10 | 114118 | C | T | upstream_gene_variant | MODIFIER | c.-3808G>A| |
S130 |
| 90124 | BAA10g00230 | A10 | 114204 | C | T | upstream_gene_variant | MODIFIER | c.-3894G>A| |
S204 |
| 90125 | BAA10g00230 | A10 | 114531 | C | T | upstream_gene_variant | MODIFIER | c.-4221G>A| |
S238 |