| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 190751 | BAA02g26050 | A02 | 14437569 | C | T | synonymous_variant | LOW | c.357G>A|p.Val119Val |
S142 |
| 190752 | BAA02g26050 | A02 | 14438585 | C | T | upstream_gene_variant | MODIFIER | c.-584G>A| |
S308 |
| 190753 | BAA02g26050 | A02 | 14439437 | G | A | upstream_gene_variant | MODIFIER | c.-1436C>T| |
S70 |
| 190754 | BAA02g26050 | A02 | 14439870 | C | T | upstream_gene_variant | MODIFIER | c.-1869G>A| |
S185 |
| 190755 | BAA02g26050 | A02 | 14440136 | C | T | upstream_gene_variant | MODIFIER | c.-2135G>A| |
S282 |
| 190756 | BAA02g26050 | A02 | 14440340 | C | T | upstream_gene_variant | MODIFIER | c.-2339G>A| |
S212 |
| 190757 | BAA02g26050 | A02 | 14440409 | G | A | upstream_gene_variant | MODIFIER | c.-2408C>T| |
S59 |
| 190758 | BAA02g26070 | A02 | 14440476 | G | A | missense_variant | MODERATE | c.364C>T|p.Leu122Phe |
S50 |
| 190759 | BAA02g26070 | A02 | 14440546 | C | T | synonymous_variant | LOW | c.294G>A|p.Ser98Ser |
S182 |
| 190760 | BAA02g26070 | A02 | 14440923 | G | A | missense_variant | MODERATE | c.8C>T|p.Ser3Leu |
S191 |
| 190761 | BAA02g26050 | A02 | 14442192 | C | T | upstream_gene_variant | MODIFIER | c.-4191G>A| |
S40 S49 |
| 190762 | BAA02g26050 | A02 | 14442849 | G | A | upstream_gene_variant | MODIFIER | c.-4848C>T| |
S197 |
| 190763 | BAA02g26050 | A02 | 14442927 | C | T | upstream_gene_variant | MODIFIER | c.-4926G>A| |
S97 |
| 190764 | BAA02g26070 | A02 | 14443200 | G | A | upstream_gene_variant | MODIFIER | c.-2270C>T| |
S25 |
| 190765 | BAA02g26070 | A02 | 14443688 | G | A | upstream_gene_variant | MODIFIER | c.-2758C>T| |
S136 |
| 190766 | BAA02g26070 | A02 | 14443900 | C | T | upstream_gene_variant | MODIFIER | c.-2970G>A| |
S274 |
| 190767 | BAA02g26070 | A02 | 14444206 | G | A | upstream_gene_variant | MODIFIER | c.-3276C>T| |
S237 |
| 190768 | BAA02g26070 | A02 | 14444362 | G | A | upstream_gene_variant | MODIFIER | c.-3432C>T| |
|
| 190769 | BAA02g26070 | A02 | 14444452 | G | A | upstream_gene_variant | MODIFIER | c.-3522C>T| |
S37 |
| 190770 | BAA02g26070 | A02 | 14444705 | G | A | upstream_gene_variant | MODIFIER | c.-3775C>T| |
S109 |
| 190771 | BAA02g26070 | A02 | 14444786 | C | T | upstream_gene_variant | MODIFIER | c.-3856G>A| |
S123 |
| 190772 | BAA02g26080 | A02 | 14446736 | C | T | upstream_gene_variant | MODIFIER | c.-365C>T| |
S61 |
| 190773 | BAA02g26080 | A02 | 14447377 | C | T | missense_variant | MODERATE | c.277C>T|p.Leu93Phe |
S192 |
| 190774 | BAA02g26080 | A02 | 14447727 | G | A | missense_variant | MODERATE | c.538G>A|p.Asp180Asn |
S28 S50 |
| 190775 | BAA02g26080 | A02 | 14447729 | C | T | synonymous_variant | LOW | c.540C>T|p.Asp180Asp |
S32 |