| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 126351 | BAA10g15140 | A10 | 15630886 | G | C | upstream_gene_variant | MODIFIER | c.-4284G>C| |
S200 |
| 126352 | BAA10g15130 | A10 | 15631505 | G | A | missense_variant | MODERATE | c.1598C>T|p.Ala533Val |
S295 |
| 126353 | BAA10g15130 | A10 | 15631569 | G | A | missense_variant | MODERATE | c.1534C>T|p.Pro512Ser |
S125 |
| 126354 | BAA10g15130 | A10 | 15631985 | C | T | missense_variant | MODERATE | c.1277G>A|p.Gly426Glu |
S70 |
| 126355 | BAA10g15140 | A10 | 15632453 | C | T | upstream_gene_variant | MODIFIER | c.-2717C>T| |
S187 |
| 126356 | BAA10g15140 | A10 | 15632495 | C | T | upstream_gene_variant | MODIFIER | c.-2675C>T| |
S8 |
| 126357 | BAA10g15130 | A10 | 15632725 | G | A | synonymous_variant | LOW | c.646C>T|p.Leu216Leu |
S95 |
| 126358 | BAA10g15130 | A10 | 15633103 | G | A | missense_variant | MODERATE | c.268C>T|p.Leu90Phe |
S9 |
| 126359 | BAA10g15130 | A10 | 15635614 | C | T | upstream_gene_variant | MODIFIER | c.-2244G>A| |
S87 |
| 126360 | BAA10g15140 | A10 | 15635767 | G | A | missense_variant | MODERATE | c.224G>A|p.Ser75Asn |
S262 |
| 126361 | BAA10g15130 | A10 | 15636274 | G | A | upstream_gene_variant | MODIFIER | c.-2904C>T| |
S166 |
| 126362 | BAA10g15140 | A10 | 15636741 | C | T | synonymous_variant | LOW | c.826C>T|p.Leu276Leu |
S20 |
| 126363 | BAA10g15140 | A10 | 15636804 | C | T | missense_variant | MODERATE | c.889C>T|p.Pro297Ser |
S210 |
| 126364 | BAA10g15140 | A10 | 15636967 | G | A | missense_variant | MODERATE | c.1052G>A|p.Gly351Glu |
S291 |
| 126365 | BAA10g15150 | A10 | 15637480 | C | T | synonymous_variant | LOW | c.2244G>A|p.Glu748Glu |
S86 |
| 126366 | BAA10g15150 | A10 | 15637527 | G | A | synonymous_variant | LOW | c.2197C>T|p.Leu733Leu |
S294 |
| 126367 | BAA10g15150 | A10 | 15637590 | G | A | synonymous_variant | LOW | c.2134C>T|p.Leu712Leu |
S151 |
| 126368 | BAA10g15150 | A10 | 15637736 | C | T | missense_variant | MODERATE | c.1988G>A|p.Arg663Lys |
S177 |
| 126369 | BAA10g15150 | A10 | 15638389 | C | T | synonymous_variant | LOW | c.1335G>A|p.Leu445Leu |
S148 S210 |
| 126370 | BAA10g15150 | A10 | 15639018 | G | A | missense_variant | MODERATE | c.706C>T|p.Leu236Phe |
S236 |
| 126371 | BAA10g15150 | A10 | 15640117 | G | A | upstream_gene_variant | MODIFIER | c.-394C>T| |
S138 |
| 126372 | BAA10g15150 | A10 | 15640203 | G | A | upstream_gene_variant | MODIFIER | c.-480C>T| |
S223 |
| 126373 | BAA10g15160 | A10 | 15641405 | G | A | synonymous_variant | LOW | c.960C>T|p.Arg320Arg |
S61 |
| 126374 | BAA10g15150 | A10 | 15642273 | C | G | upstream_gene_variant | MODIFIER | c.-2550G>C| |
S176 |
| 126375 | BAA10g15150 | A10 | 15642324 | C | T | upstream_gene_variant | MODIFIER | c.-2601G>A| |
S191 |