| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 112151 | BAA10g08460 | A10 | 10252971 | G | A | downstream_gene_variant | MODIFIER | c.*2624G>A| |
S105 S106 |
| 112152 | BAA10g08460 | A10 | 10253011 | C | T | downstream_gene_variant | MODIFIER | c.*2664C>T| |
S37 |
| 112153 | BAA10g08470 | A10 | 10253122 | G | A | missense_variant | MODERATE | c.829G>A|p.Glu277Lys |
S179 |
| 112154 | BAA10g08460 | A10 | 10253686 | G | A | downstream_gene_variant | MODIFIER | c.*3339G>A| |
S65 |
| 112155 | BAA10g08460 | A10 | 10254125 | C | T | downstream_gene_variant | MODIFIER | c.*3778C>T| |
S153 S213 |
| 112156 | BAA10g08460 | A10 | 10254722 | G | A | downstream_gene_variant | MODIFIER | c.*4375G>A| |
S94 |
| 112157 | BAA10g08460 | A10 | 10254736 | G | A | downstream_gene_variant | MODIFIER | c.*4389G>A| |
S4 |
| 112158 | BAA10g08470 | A10 | 10255649 | C | T | synonymous_variant | LOW | c.1929C>T|p.Pro643Pro |
S235 |
| 112159 | BAA10g08490 | A10 | 10257738 | C | T | upstream_gene_variant | MODIFIER | c.-3669C>T| |
S249 |
| 112160 | BAA10g08490 | A10 | 10258011 | C | T | upstream_gene_variant | MODIFIER | c.-3396C>T| |
S177 |
| 112161 | BAA10g08490 | A10 | 10258039 | G | A | upstream_gene_variant | MODIFIER | c.-3368G>A| |
S129 |
| 112162 | BAA10g08490 | A10 | 10258307 | C | T | upstream_gene_variant | MODIFIER | c.-3100C>T| |
S176 |
| 112163 | BAA10g08490 | A10 | 10258709 | G | A | upstream_gene_variant | MODIFIER | c.-2698G>A| |
S100 |
| 112164 | BAA10g08480 | A10 | 10260005 | G | A | synonymous_variant | LOW | c.201C>T|p.Phe67Phe |
S71 |
| 112165 | BAA10g08480 | A10 | 10260363 | G | A | upstream_gene_variant | MODIFIER | c.-158C>T| |
S221 |
| 112166 | BAA10g08490 | A10 | 10261871 | C | T | missense_variant | MODERATE | c.221C>T|p.Pro74Leu |
S208 S93 |
| 112167 | BAA10g08490 | A10 | 10262574 | G | A | missense_variant | MODERATE | c.559G>A|p.Glu187Lys |
S138 |
| 112168 | BAA10g08490 | A10 | 10262601 | G | T | stop_gained | HIGH | c.586G>T|p.Gly196* |
S9 |
| 112169 | BAA10g08480 | A10 | 10263586 | C | T | upstream_gene_variant | MODIFIER | c.-3381G>A| |
S247 |
| 112170 | BAA10g08500 | A10 | 10264172 | G | A | missense_variant | MODERATE | c.427G>A|p.Glu143Lys |
S150 |
| 112171 | BAA10g08500 | A10 | 10264211 | G | A | missense_variant | MODERATE | c.466G>A|p.Ala156Thr |
S150 |
| 112172 | BAA10g08500 | A10 | 10265008 | G | A | missense_variant | MODERATE | c.920G>A|p.Cys307Tyr |
S65 |
| 112173 | BAA10g08490 | A10 | 10265235 | C | T | downstream_gene_variant | MODIFIER | c.*2542C>T| |
S187 |
| 112174 | BAA10g08490 | A10 | 10265512 | G | A | downstream_gene_variant | MODIFIER | c.*2819G>A| |
S207 |
| 112175 | BAA10g08490 | A10 | 10265626 | C | T | downstream_gene_variant | MODIFIER | c.*2933C>T| |
S146 |