| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 75251 | BAA01g39640 | A01 | 26336164 | G | A | upstream_gene_variant | MODIFIER | c.-2921C>T| |
S5 |
| 75252 | BAA01g39640 | A01 | 26337802 | C | T | upstream_gene_variant | MODIFIER | c.-4559G>A| |
S289 S290 |
| 75253 | BAA01g39650 | A01 | 26338674 | G | A | upstream_gene_variant | MODIFIER | c.-2922C>T| |
S140 |
| 75254 | BAA01g39660 | A01 | 26339503 | G | A | missense_variant | MODERATE | c.860G>A|p.Gly287Glu |
S169 |
| 75255 | BAA01g39660 | A01 | 26339795 | G | A | missense_variant | MODERATE | c.1075G>A|p.Val359Met |
S5 |
| 75256 | BAA01g39670 | A01 | 26341171 | C | T | missense_variant | MODERATE | c.46C>T|p.Leu16Phe |
S266 |
| 75257 | BAA01g39670 | A01 | 26341244 | C | T | missense_variant | MODERATE | c.119C>T|p.Ser40Phe |
S39 |
| 75258 | BAA01g39670 | A01 | 26341356 | C | T | synonymous_variant | LOW | c.231C>T|p.Val77Val |
S62 |
| 75259 | BAA01g39670 | A01 | 26341385 | C | T | missense_variant | MODERATE | c.260C>T|p.Ser87Phe |
S159 S243 |
| 75260 | BAA01g39670 | A01 | 26341659 | C | T | synonymous_variant | LOW | c.534C>T|p.Ser178Ser |
S59 |
| 75261 | BAA01g39670 | A01 | 26341999 | C | T | missense_variant | MODERATE | c.874C>T|p.Pro292Ser |
S161 |
| 75262 | BAA01g39670 | A01 | 26342212 | C | T | synonymous_variant | LOW | c.1087C>T|p.Leu363Leu |
S293 |
| 75263 | BAA01g39670 | A01 | 26342352 | C | T | synonymous_variant | LOW | c.1227C>T|p.Asn409Asn |
S234 |
| 75264 | BAA01g39670 | A01 | 26342852 | C | T | missense_variant | MODERATE | c.1727C>T|p.Thr576Ile |
S166 |
| 75265 | BAA01g39670 | A01 | 26343043 | C | T | synonymous_variant | LOW | c.1918C>T|p.Leu640Leu |
S63 |
| 75266 | BAA01g39660 | A01 | 26343656 | C | T | downstream_gene_variant | MODIFIER | c.*3106C>T| |
S288 |
| 75267 | BAA01g39680 | A01 | 26351781 | G | A | downstream_gene_variant | MODIFIER | c.*1426G>A| |
S189 |
| 75268 | BAA01g39680 | A01 | 26351942 | G | A | downstream_gene_variant | MODIFIER | c.*1587G>A| |
S271 |
| 75269 | BAA01g39690 | A01 | 26352560 | C | T | missense_variant | MODERATE | c.814G>A|p.Val272Ile |
S50 |
| 75270 | BAA01g39690 | A01 | 26353683 | G | A | synonymous_variant | LOW | c.81C>T|p.Val27Val |
S294 |
| 75271 | BAA01g39690 | A01 | 26353729 | C | T | missense_variant | MODERATE | c.35G>A|p.Ser12Asn |
S176 |
| 75272 | BAA01g39690 | A01 | 26353944 | C | T | upstream_gene_variant | MODIFIER | c.-181G>A| |
S289 S290 |
| 75273 | BAA01g39690 | A01 | 26354068 | G | A | upstream_gene_variant | MODIFIER | c.-305C>T| |
S252 |
| 75274 | BAA01g39690 | A01 | 26354743 | G | A | upstream_gene_variant | MODIFIER | c.-980C>T| |
S246 |
| 75275 | BAA01g39690 | A01 | 26355998 | G | A | upstream_gene_variant | MODIFIER | c.-2235C>T| |
S116 |