| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 126451 | BAA10g15220 | A10 | 15657488 | G | A | upstream_gene_variant | MODIFIER | c.-933G>A| |
S293 |
| 126452 | BAA10g15210 | A10 | 15658412 | C | T | upstream_gene_variant | MODIFIER | c.-507G>A| |
S202 |
| 126453 | BAA10g15220 | A10 | 15659810 | C | T | missense_variant | MODERATE | c.478C>T|p.Pro160Ser |
S45 |
| 126454 | BAA10g15210 | A10 | 15659984 | G | A | upstream_gene_variant | MODIFIER | c.-2079C>T| |
S290 S85 |
| 126455 | BAA10g15220 | A10 | 15660241 | C | T | synonymous_variant | LOW | c.648C>T|p.Tyr216Tyr |
S113 |
| 126456 | BAA10g15220 | A10 | 15660286 | G | A | synonymous_variant | LOW | c.693G>A|p.Lys231Lys |
S39 |
| 126457 | BAA10g15210 | A10 | 15661208 | C | T | upstream_gene_variant | MODIFIER | c.-3303G>A| |
S281 |
| 126458 | BAA10g15230 | A10 | 15663841 | G | A | upstream_gene_variant | MODIFIER | c.-4616G>A| |
S169 S45 |
| 126459 | BAA10g15230 | A10 | 15665224 | T | G | upstream_gene_variant | MODIFIER | c.-3233T>G| |
S148 S20 |
| 126460 | BAA10g15230 | A10 | 15665811 | C | T | upstream_gene_variant | MODIFIER | c.-2646C>T| |
S11 |
| 126461 | BAA10g15230 | A10 | 15667890 | G | A | upstream_gene_variant | MODIFIER | c.-567G>A| |
S265 |
| 126462 | BAA10g15240 | A10 | 15668700 | A | G | downstream_gene_variant | MODIFIER | c.*1712T>C| |
S99 |
| 126463 | BAA10g15240 | A10 | 15668825 | C | T | downstream_gene_variant | MODIFIER | c.*1587G>A| |
S156 |
| 126464 | BAA10g15240 | A10 | 15671561 | G | A | upstream_gene_variant | MODIFIER | c.-988C>T| |
S139 |
| 126465 | BAA10g15240 | A10 | 15672072 | C | T | upstream_gene_variant | MODIFIER | c.-1499G>A| |
S294 |
| 126466 | BAA10g15240 | A10 | 15673665 | C | T | upstream_gene_variant | MODIFIER | c.-3092G>A| |
S38 |
| 126467 | BAA10g15240 | A10 | 15674909 | G | A | upstream_gene_variant | MODIFIER | c.-4336C>T| |
S192 |
| 126468 | BAA10g15250 | A10 | 15676281 | G | A | synonymous_variant | LOW | c.135G>A|p.Arg45Arg |
S100 |
| 126469 | BAA10g15250 | A10 | 15676735 | C | T | missense_variant | MODERATE | c.343C>T|p.Pro115Ser |
S249 |
| 126470 | BAA10g15260 | A10 | 15678972 | C | T | missense_variant | MODERATE | c.2752G>A|p.Ala918Thr |
S140 |
| 126471 | BAA10g15260 | A10 | 15679081 | G | A | synonymous_variant | LOW | c.2643C>T|p.Leu881Leu |
S112 |
| 126472 | BAA10g15260 | A10 | 15679770 | G | A | missense_variant&splice_region_variant | MODERATE | c.2224C>T|p.Pro742Ser |
S120 |
| 126473 | BAA10g15250 | A10 | 15680069 | G | A | downstream_gene_variant | MODIFIER | c.*3266G>A| |
S72 S78 |
| 126474 | BAA10g15260 | A10 | 15680091 | C | T | splice_region_variant&intron_variant | LOW | c.1983+5G>A| |
S25 |
| 126475 | BAA10g15260 | A10 | 15680288 | C | T | synonymous_variant | LOW | c.1878G>A|p.Glu626Glu |
S144 |