| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 168551 | BAA02g13810 | A02 | 6453993 | G | A | intron_variant | MODIFIER | c.65-166C>T| |
S231 |
| 168552 | BAA02g13810 | A02 | 6454017 | G | A | intron_variant | MODIFIER | c.65-190C>T| |
S210 S225 |
| 168553 | BAA02g13810 | A02 | 6454801 | G | A | upstream_gene_variant | MODIFIER | c.-382C>T| |
S36 |
| 168554 | BAA02g13810 | A02 | 6457584 | G | A | upstream_gene_variant | MODIFIER | c.-3165C>T| |
S57 |
| 168555 | BAA02g13810 | A02 | 6458757 | G | A | upstream_gene_variant | MODIFIER | c.-4338C>T| |
S271 |
| 168556 | BAA02g13810 | A02 | 6458804 | G | A | upstream_gene_variant | MODIFIER | c.-4385C>T| |
S110 |
| 168557 | BAA02g13820 | A02 | 6459572 | C | T | upstream_gene_variant | MODIFIER | c.-239C>T| |
S249 |
| 168558 | BAA02g13820 | A02 | 6459986 | G | A | missense_variant | MODERATE | c.176G>A|p.Ser59Asn |
S252 |
| 168559 | BAA02g13830 | A02 | 6460587 | A | T | upstream_gene_variant | MODIFIER | c.-1847A>T| |
S303 |
| 168560 | BAA02g13830 | A02 | 6461160 | G | A | upstream_gene_variant | MODIFIER | c.-1274G>A| |
S64 |
| 168561 | BAA02g13830 | A02 | 6461342 | C | T | upstream_gene_variant | MODIFIER | c.-1092C>T| |
S218 |
| 168562 | BAA02g13830 | A02 | 6462111 | G | A | upstream_gene_variant | MODIFIER | c.-323G>A| |
S184 |
| 168563 | BAA02g13830 | A02 | 6462449 | C | T | synonymous_variant | LOW | c.16C>T|p.Leu6Leu |
S135 |
| 168564 | BAA02g13830 | A02 | 6463616 | G | A | synonymous_variant | LOW | c.1101G>A|p.Ser367Ser |
S168 |
| 168565 | BAA02g13840 | A02 | 6465005 | C | T | missense_variant | MODERATE | c.214C>T|p.His72Tyr |
S9 |
| 168566 | BAA02g13850 | A02 | 6466269 | G | A | upstream_gene_variant | MODIFIER | c.-1696G>A| |
S136 |
| 168567 | BAA02g13850 | A02 | 6466541 | G | A | upstream_gene_variant | MODIFIER | c.-1424G>A| |
S162 |
| 168568 | BAA02g13850 | A02 | 6467333 | G | A | upstream_gene_variant | MODIFIER | c.-632G>A| |
S52 |
| 168569 | BAA02g13860 | A02 | 6470986 | C | T | missense_variant | MODERATE | c.779C>T|p.Ser260Phe |
S115 |
| 168570 | BAA02g13870 | A02 | 6472201 | C | T | missense_variant | MODERATE | c.145G>A|p.Val49Met |
S230 |
| 168571 | BAA02g13870 | A02 | 6472383 | C | T | upstream_gene_variant | MODIFIER | c.-38G>A| |
S58 |
| 168572 | BAA02g13870 | A02 | 6472674 | C | T | upstream_gene_variant | MODIFIER | c.-329G>A| |
S99 |
| 168573 | BAA02g13870 | A02 | 6472731 | C | T | upstream_gene_variant | MODIFIER | c.-386G>A| |
S177 |
| 168574 | BAA02g13870 | A02 | 6473300 | C | T | upstream_gene_variant | MODIFIER | c.-955G>A| |
S103 |
| 168575 | BAA02g13870 | A02 | 6474488 | G | A | upstream_gene_variant | MODIFIER | c.-2143C>T| |
S280 |