| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 149551 | BAA10g33660 | A10 | 23904308 | G | A | intron_variant | MODIFIER | c.850-206C>T| |
S286 |
| 149552 | BAA10g33660 | A10 | 23904708 | C | T | missense_variant | MODERATE | c.715G>A|p.Gly239Arg |
S148 S210 S30 S31 |
| 149553 | BAA10g33660 | A10 | 23905419 | C | T | missense_variant | MODERATE | c.4G>A|p.Ala2Thr |
S80 |
| 149554 | BAA10g33660 | A10 | 23906153 | C | T | upstream_gene_variant | MODIFIER | c.-731G>A| |
S244 |
| 149555 | BAA10g33660 | A10 | 23907383 | G | A | upstream_gene_variant | MODIFIER | c.-1961C>T| |
S45 |
| 149556 | BAA10g33660 | A10 | 23907647 | G | A | upstream_gene_variant | MODIFIER | c.-2225C>T| |
S17 |
| 149557 | BAA10g33660 | A10 | 23907715 | G | A | upstream_gene_variant | MODIFIER | c.-2293C>T| |
S140 S168 S278 S64 |
| 149558 | BAA10g33670 | A10 | 23911192 | C | T | downstream_gene_variant | MODIFIER | c.*972G>A| |
S33 |
| 149559 | BAA10g33680 | A10 | 23912566 | C | T | downstream_gene_variant | MODIFIER | c.*1516G>A| |
S2 |
| 149560 | BAA10g33680 | A10 | 23912575 | G | A | downstream_gene_variant | MODIFIER | c.*1507C>T| |
S289 S290 |
| 149561 | BAA10g33680 | A10 | 23912964 | C | T | downstream_gene_variant | MODIFIER | c.*1118G>A| |
S305 |
| 149562 | BAA10g33680 | A10 | 23914160 | G | A | synonymous_variant | LOW | c.2436C>T|p.Tyr812Tyr |
S299 |
| 149563 | BAA10g33670 | A10 | 23914219 | G | A | upstream_gene_variant | MODIFIER | c.-604C>T| |
S166 |
| 149564 | BAA10g33680 | A10 | 23914737 | C | T | missense_variant | MODERATE | c.2095G>A|p.Asp699Asn |
S5 |
| 149565 | BAA10g33680 | A10 | 23915678 | G | A | missense_variant | MODERATE | c.1562C>T|p.Pro521Leu |
S179 |
| 149566 | BAA10g33680 | A10 | 23915720 | G | A | missense_variant | MODERATE | c.1520C>T|p.Thr507Ile |
S94 |
| 149567 | BAA10g33670 | A10 | 23916020 | G | A | upstream_gene_variant | MODIFIER | c.-2405C>T| |
S263 |
| 149568 | BAA10g33680 | A10 | 23916208 | G | A | splice_region_variant&synonymous_variant | LOW | c.1218C>T|p.Ser406Ser |
S32 |
| 149569 | BAA10g33680 | A10 | 23919418 | C | T | splice_donor_variant&intron_variant | HIGH | c.136+1G>A| |
S225 S73 |
| 149570 | BAA10g33680 | A10 | 23919833 | C | T | upstream_gene_variant | MODIFIER | c.-279G>A| |
S277 |
| 149571 | BAA10g33680 | A10 | 23920473 | G | A | upstream_gene_variant | MODIFIER | c.-919C>T| |
S99 |
| 149572 | BAA10g33690 | A10 | 23920746 | C | T | missense_variant | MODERATE | c.2455G>A|p.Asp819Asn |
S61 |
| 149573 | BAA10g33690 | A10 | 23922696 | C | T | missense_variant | MODERATE | c.865G>A|p.Val289Ile |
S123 |
| 149574 | BAA10g33690 | A10 | 23922861 | C | T | missense_variant | MODERATE | c.700G>A|p.Val234Met |
S282 |
| 149575 | BAA10g33690 | A10 | 23923113 | C | T | missense_variant | MODERATE | c.448G>A|p.Gly150Arg |
S250 |