| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 15951 | BAA01g12150 | A01 | 5702959 | G | A | missense_variant | MODERATE | c.427G>A|p.Asp143Asn |
S197 |
| 15952 | BAA01g12140 | A01 | 5703365 | G | A | upstream_gene_variant | MODIFIER | c.-3889C>T| |
S6 |
| 15953 | BAA01g12140 | A01 | 5704001 | C | T | upstream_gene_variant | MODIFIER | c.-4525G>A| |
S71 |
| 15954 | BAA01g12160 | A01 | 5705013 | G | A | upstream_gene_variant | MODIFIER | c.-22G>A| |
S17 |
| 15955 | BAA01g12150 | A01 | 5706955 | G | A | downstream_gene_variant | MODIFIER | c.*3757G>A| |
S124 |
| 15956 | BAA01g12170 | A01 | 5707635 | C | T | missense_variant | MODERATE | c.1399G>A|p.Val467Ile |
S36 |
| 15957 | BAA01g12170 | A01 | 5707802 | C | T | missense_variant | MODERATE | c.1232G>A|p.Gly411Glu |
S44 |
| 15958 | BAA01g12150 | A01 | 5707851 | C | T | downstream_gene_variant | MODIFIER | c.*4653C>T| |
S289 S290 |
| 15959 | BAA01g12170 | A01 | 5708060 | G | A | synonymous_variant | LOW | c.1143C>T|p.Phe381Phe |
S238 |
| 15960 | BAA01g12170 | A01 | 5709079 | C | T | synonymous_variant | LOW | c.525G>A|p.Lys175Lys |
S36 |
| 15961 | BAA01g12170 | A01 | 5709247 | C | T | missense_variant | MODERATE | c.431G>A|p.Gly144Asp |
S152 |
| 15962 | BAA01g12170 | A01 | 5709837 | C | T | synonymous_variant | LOW | c.18G>A|p.Glu6Glu |
S169 |
| 15963 | BAA01g12170 | A01 | 5710045 | G | A | upstream_gene_variant | MODIFIER | c.-191C>T| |
S87 |
| 15964 | BAA01g12170 | A01 | 5710108 | G | A | upstream_gene_variant | MODIFIER | c.-254C>T| |
S157 |
| 15965 | BAA01g12170 | A01 | 5711450 | C | T | upstream_gene_variant | MODIFIER | c.-1596G>A| |
S161 |
| 15966 | BAA01g12170 | A01 | 5711964 | G | A | upstream_gene_variant | MODIFIER | c.-2110C>T| |
S193 |
| 15967 | BAA01g12180 | A01 | 5712324 | C | T | missense_variant | MODERATE | c.7007G>A|p.Arg2336Gln |
S221 |
| 15968 | BAA01g12170 | A01 | 5713158 | G | A | upstream_gene_variant | MODIFIER | c.-3304C>T| |
S156 |
| 15969 | BAA01g12180 | A01 | 5713231 | C | T | missense_variant | MODERATE | c.6361G>A|p.Asp2121Asn |
S120 |
| 15970 | BAA01g12170 | A01 | 5713773 | G | A | upstream_gene_variant | MODIFIER | c.-3919C>T| |
S105 S106 |
| 15971 | BAA01g12180 | A01 | 5714200 | C | T | synonymous_variant | LOW | c.5628G>A|p.Arg1876Arg |
S128 |
| 15972 | BAA01g12170 | A01 | 5714391 | G | A | upstream_gene_variant | MODIFIER | c.-4537C>T| |
S197 |
| 15973 | BAA01g12180 | A01 | 5714830 | G | A | missense_variant | MODERATE | c.5216C>T|p.Ser1739Phe |
S12 |
| 15974 | BAA01g12180 | A01 | 5714989 | G | A | missense_variant | MODERATE | c.5144C>T|p.Thr1715Ile |
S188 |
| 15975 | BAA01g12180 | A01 | 5716058 | A | T | intron_variant | MODIFIER | c.4306-105T>A| |
S95 |