| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 11651 | BAA01g09320 | A01 | 4154181 | G | A | missense_variant | MODERATE | c.1280C>T|p.Ala427Val |
S33 |
| 11652 | BAA01g09320 | A01 | 4155105 | G | A | missense_variant | MODERATE | c.356C>T|p.Pro119Leu |
S207 |
| 11653 | BAA01g09320 | A01 | 4155118 | C | T | missense_variant | MODERATE | c.343G>A|p.Gly115Arg |
S176 |
| 11654 | BAA01g09320 | A01 | 4157059 | G | A | upstream_gene_variant | MODIFIER | c.-1599C>T| |
S279 |
| 11655 | BAA01g09330 | A01 | 4157090 | C | T | splice_region_variant&synonymous_variant | LOW | c.1116G>A|p.Lys372Lys |
S225 S73 |
| 11656 | BAA01g09320 | A01 | 4157989 | G | A | upstream_gene_variant | MODIFIER | c.-2529C>T| |
S45 |
| 11657 | BAA01g09320 | A01 | 4159471 | C | T | upstream_gene_variant | MODIFIER | c.-4011G>A| |
S242 |
| 11658 | BAA01g09340 | A01 | 4160209 | C | T | missense_variant | MODERATE | c.524C>T|p.Ser175Phe |
S275 |
| 11659 | BAA01g09340 | A01 | 4160391 | C | T | missense_variant | MODERATE | c.706C>T|p.Pro236Ser |
S100 |
| 11660 | BAA01g09340 | A01 | 4160412 | G | A | missense_variant | MODERATE | c.727G>A|p.Asp243Asn |
S129 |
| 11661 | BAA01g09340 | A01 | 4161323 | C | T | missense_variant | MODERATE | c.1607C>T|p.Ala536Val |
S189 |
| 11662 | BAA01g09350 | A01 | 4161956 | C | T | missense_variant | MODERATE | c.1184G>A|p.Gly395Glu |
S282 |
| 11663 | BAA01g09350 | A01 | 4162011 | G | A | synonymous_variant | LOW | c.1129C>T|p.Leu377Leu |
S293 |
| 11664 | BAA01g09350 | A01 | 4162018 | C | T | synonymous_variant | LOW | c.1122G>A|p.Lys374Lys |
S189 |
| 11665 | BAA01g09330 | A01 | 4162059 | C | T | upstream_gene_variant | MODIFIER | c.-3523G>A| |
S19 |
| 11666 | BAA01g09350 | A01 | 4162157 | G | A | missense_variant | MODERATE | c.1070C>T|p.Pro357Leu |
S168 |
| 11667 | BAA01g09350 | A01 | 4162284 | G | A | missense_variant | MODERATE | c.943C>T|p.Leu315Phe |
S69 |
| 11668 | BAA01g09330 | A01 | 4162611 | G | A | upstream_gene_variant | MODIFIER | c.-4075C>T| |
S217 |
| 11669 | BAA01g09330 | A01 | 4162919 | C | T | upstream_gene_variant | MODIFIER | c.-4383G>A| |
S19 |
| 11670 | BAA01g09330 | A01 | 4163074 | G | A | upstream_gene_variant | MODIFIER | c.-4538C>T| |
S84 |
| 11671 | BAA01g09350 | A01 | 4163620 | G | A | missense_variant | MODERATE | c.326C>T|p.Pro109Leu |
S32 |
| 11672 | BAA01g09350 | A01 | 4163672 | C | T | missense_variant | MODERATE | c.274G>A|p.Glu92Lys |
S19 |
| 11673 | BAA01g09350 | A01 | 4163862 | C | T | synonymous_variant | LOW | c.84G>A|p.Glu28Glu |
S18 |
| 11674 | BAA01g09350 | A01 | 4164106 | C | T | upstream_gene_variant | MODIFIER | c.-161G>A| |
S61 |
| 11675 | BAA01g09350 | A01 | 4165861 | G | A | upstream_gene_variant | MODIFIER | c.-1916C>T| |
S173 |