| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 139501 | BAA10g24730 | A10 | 20273118 | C | A | missense_variant | MODERATE | c.768G>T|p.Glu256Asp |
S279 |
| 139502 | BAA10g24720 | A10 | 20273488 | C | T | upstream_gene_variant | MODIFIER | c.-2813G>A| |
S18 |
| 139503 | BAA10g24720 | A10 | 20274571 | G | A | upstream_gene_variant | MODIFIER | c.-3896C>T| |
S156 |
| 139504 | BAA10g24730 | A10 | 20274770 | G | A | synonymous_variant | LOW | c.531C>T|p.Phe177Phe |
S1 S90 |
| 139505 | BAA10g24730 | A10 | 20275098 | G | A | splice_region_variant&intron_variant | LOW | c.272+6C>T| |
S197 |
| 139506 | BAA10g24720 | A10 | 20275576 | C | T | upstream_gene_variant | MODIFIER | c.-4901G>A| |
S33 |
| 139507 | BAA10g24730 | A10 | 20276360 | C | T | upstream_gene_variant | MODIFIER | c.-345G>A| |
S96 |
| 139508 | BAA10g24730 | A10 | 20277394 | G | A | upstream_gene_variant | MODIFIER | c.-1379C>T| |
S84 S93 |
| 139509 | BAA10g24730 | A10 | 20277795 | C | T | upstream_gene_variant | MODIFIER | c.-1780G>A| |
S45 |
| 139510 | BAA10g24730 | A10 | 20278838 | G | A | upstream_gene_variant | MODIFIER | c.-2823C>T| |
S179 |
| 139511 | BAA10g24730 | A10 | 20279175 | C | T | upstream_gene_variant | MODIFIER | c.-3160G>A| |
S58 |
| 139512 | BAA10g24740 | A10 | 20280291 | G | A | missense_variant | MODERATE | c.656C>T|p.Pro219Leu |
S1 S90 |
| 139513 | BAA10g24740 | A10 | 20281264 | C | T | missense_variant | MODERATE | c.523G>A|p.Gly175Ser |
S19 |
| 139514 | BAA10g24740 | A10 | 20281826 | C | T | synonymous_variant | LOW | c.126G>A|p.Lys42Lys |
S282 |
| 139515 | BAA10g24740 | A10 | 20282532 | G | A | upstream_gene_variant | MODIFIER | c.-581C>T| |
S57 |
| 139516 | BAA10g24740 | A10 | 20283060 | C | T | upstream_gene_variant | MODIFIER | c.-1109G>A| |
S44 |
| 139517 | BAA10g24740 | A10 | 20285386 | G | A | upstream_gene_variant | MODIFIER | c.-3435C>T| |
S241 |
| 139518 | BAA10g24750 | A10 | 20286272 | G | A | missense_variant | MODERATE | c.1217C>T|p.Thr406Ile |
S59 |
| 139519 | BAA10g24750 | A10 | 20287021 | G | A | missense_variant | MODERATE | c.616C>T|p.Arg206Cys |
S122 |
| 139520 | BAA10g24750 | A10 | 20287210 | G | A | missense_variant | MODERATE | c.427C>T|p.Pro143Ser |
S142 |
| 139521 | BAA10g24750 | A10 | 20287347 | G | A | missense_variant | MODERATE | c.290C>T|p.Thr97Ile |
S120 |
| 139522 | BAA10g24750 | A10 | 20287421 | C | T | synonymous_variant | LOW | c.216G>A|p.Thr72Thr |
S162 |
| 139523 | BAA10g24750 | A10 | 20287622 | C | T | missense_variant | MODERATE | c.107G>A|p.Arg36Gln |
S44 |
| 139524 | BAA10g24750 | A10 | 20288465 | C | T | upstream_gene_variant | MODIFIER | c.-737G>A| |
S171 |
| 139525 | BAA10g24750 | A10 | 20289615 | G | A | upstream_gene_variant | MODIFIER | c.-1887C>T| |
S303 |