| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 145501 | BAA10g30040 | A10 | 22392411 | C | T | downstream_gene_variant | MODIFIER | c.*3525C>T| |
S243 |
| 145502 | BAA10g30060 | A10 | 22392616 | C | T | missense_variant | MODERATE | c.482C>T|p.Pro161Leu |
S229 |
| 145503 | BAA10g30060 | A10 | 22393724 | G | A | synonymous_variant | LOW | c.1353G>A|p.Leu451Leu |
S278 |
| 145504 | BAA10g30060 | A10 | 22393973 | G | A | synonymous_variant | LOW | c.1602G>A|p.Gln534Gln |
S241 |
| 145505 | BAA10g30050 | A10 | 22394224 | C | T | downstream_gene_variant | MODIFIER | c.*2927C>T| |
S97 |
| 145506 | BAA10g30050 | A10 | 22394929 | C | T | downstream_gene_variant | MODIFIER | c.*3632C>T| |
S34 |
| 145507 | BAA10g30070 | A10 | 22396767 | G | A | upstream_gene_variant | MODIFIER | c.-1000C>T| |
S39 |
| 145508 | BAA10g30080 | A10 | 22397137 | G | A | stop_gained | HIGH | c.2794C>T|p.Gln932* |
S270 |
| 145509 | BAA10g30080 | A10 | 22397180 | G | A | synonymous_variant | LOW | c.2751C>T|p.Leu917Leu |
S118 |
| 145510 | BAA10g30080 | A10 | 22397214 | C | T | missense_variant | MODERATE | c.2717G>A|p.Arg906Lys |
S266 |
| 145511 | BAA10g30080 | A10 | 22397654 | C | T | missense_variant | MODERATE | c.2354G>A|p.Gly785Glu |
S259 |
| 145512 | BAA10g30080 | A10 | 22397775 | C | T | missense_variant | MODERATE | c.2233G>A|p.Asp745Asn |
S230 |
| 145513 | BAA10g30080 | A10 | 22397802 | C | T | missense_variant | MODERATE | c.2206G>A|p.Gly736Ser |
S68 |
| 145514 | BAA10g30080 | A10 | 22398614 | G | A | missense_variant | MODERATE | c.1592C>T|p.Ser531Phe |
S150 |
| 145515 | BAA10g30070 | A10 | 22398935 | G | A | upstream_gene_variant | MODIFIER | c.-3168C>T| |
S134 |
| 145516 | BAA10g30080 | A10 | 22399235 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.1296-1G>A| |
S174 S27 |
| 145517 | BAA10g30070 | A10 | 22399773 | G | A | upstream_gene_variant | MODIFIER | c.-4006C>T| |
S54 |
| 145518 | BAA10g30080 | A10 | 22400930 | C | T | missense_variant | MODERATE | c.533G>A|p.Gly178Asp |
S112 |
| 145519 | BAA10g30080 | A10 | 22402108 | C | T | missense_variant | MODERATE | c.50G>A|p.Cys17Tyr |
S211 |
| 145520 | BAA10g30080 | A10 | 22402742 | C | T | upstream_gene_variant | MODIFIER | c.-585G>A| |
S174 S27 |
| 145521 | BAA10g30080 | A10 | 22402911 | G | A | upstream_gene_variant | MODIFIER | c.-754C>T| |
S118 |
| 145522 | BAA10g30080 | A10 | 22403451 | C | T | upstream_gene_variant | MODIFIER | c.-1294G>A| |
S33 |
| 145523 | BAA10g30080 | A10 | 22403885 | C | T | upstream_gene_variant | MODIFIER | c.-1728G>A| |
S256 |
| 145524 | BAA10g30080 | A10 | 22404564 | C | T | upstream_gene_variant | MODIFIER | c.-2407G>A| |
S168 S224 |
| 145525 | BAA10g30080 | A10 | 22404808 | G | A | upstream_gene_variant | MODIFIER | c.-2651C>T| |
S32 |