| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 156601 | BAA02g04560 | A02 | 1985328 | C | T | upstream_gene_variant | MODIFIER | c.-4706G>A| |
S174 S39 |
| 156602 | BAA02g04580 | A02 | 1986377 | G | A | missense_variant | MODERATE | c.275C>T|p.Pro92Leu |
S59 |
| 156603 | BAA02g04580 | A02 | 1986840 | C | T | upstream_gene_variant | MODIFIER | c.-189G>A| |
S1 S90 |
| 156604 | BAA02g04590 | A02 | 1987715 | C | T | missense_variant | MODERATE | c.1546G>A|p.Glu516Lys |
S38 |
| 156605 | BAA02g04590 | A02 | 1987847 | G | A | missense_variant | MODERATE | c.1414C>T|p.Leu472Phe |
S148 S210 S30 S31 |
| 156606 | BAA02g04590 | A02 | 1987912 | C | T | missense_variant | MODERATE | c.1349G>A|p.Gly450Glu |
S186 |
| 156607 | BAA02g04590 | A02 | 1989270 | G | A | synonymous_variant | LOW | c.303C>T|p.Tyr101Tyr |
S295 |
| 156608 | BAA02g04590 | A02 | 1989609 | C | T | missense_variant | MODERATE | c.124G>A|p.Asp42Asn |
S245 |
| 156609 | BAA02g04590 | A02 | 1989661 | C | T | synonymous_variant | LOW | c.72G>A|p.Lys24Lys |
S95 |
| 156610 | BAA02g04580 | A02 | 1990715 | C | T | upstream_gene_variant | MODIFIER | c.-4064G>A| |
S100 |
| 156611 | BAA02g04600 | A02 | 1992616 | G | A | missense_variant | MODERATE | c.146C>T|p.Ala49Val |
S107 |
| 156612 | BAA02g04590 | A02 | 1992998 | C | T | upstream_gene_variant | MODIFIER | c.-3266G>A| |
S152 |
| 156613 | BAA02g04590 | A02 | 1993021 | C | T | upstream_gene_variant | MODIFIER | c.-3289G>A| |
S58 |
| 156614 | BAA02g04590 | A02 | 1993525 | C | T | upstream_gene_variant | MODIFIER | c.-3793G>A| |
S75 |
| 156615 | BAA02g04600 | A02 | 1995378 | G | A | upstream_gene_variant | MODIFIER | c.-2617C>T| |
S87 |
| 156616 | BAA02g04600 | A02 | 1995585 | G | A | upstream_gene_variant | MODIFIER | c.-2824C>T| |
S223 |
| 156617 | BAA02g04600 | A02 | 1996014 | G | A | upstream_gene_variant | MODIFIER | c.-3253C>T| |
S156 |
| 156618 | BAA02g04610 | A02 | 1998417 | C | T | upstream_gene_variant | MODIFIER | c.-1446G>A| |
S274 |
| 156619 | BAA02g04620 | A02 | 1999492 | C | T | synonymous_variant | LOW | c.87C>T|p.Thr29Thr |
S104 |
| 156620 | BAA02g04620 | A02 | 2000185 | G | A | synonymous_variant | LOW | c.780G>A|p.Lys260Lys |
S293 |
| 156621 | BAA02g04620 | A02 | 2000216 | G | A | missense_variant | MODERATE | c.811G>A|p.Glu271Lys |
S132 S137 S215 |
| 156622 | BAA02g04620 | A02 | 2000268 | G | A | missense_variant | MODERATE | c.863G>A|p.Gly288Asp |
S266 |
| 156623 | BAA02g04610 | A02 | 2000721 | C | T | upstream_gene_variant | MODIFIER | c.-3750G>A| |
S267 |
| 156624 | BAA02g04610 | A02 | 2001489 | G | A | upstream_gene_variant | MODIFIER | c.-4518C>T| |
S177 |
| 156625 | BAA02g04610 | A02 | 2001512 | C | T | upstream_gene_variant | MODIFIER | c.-4541G>A| |
S172 |