| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 51751 | BAA01g28610 | A01 | 17940387 | G | A | missense_variant | MODERATE | c.1262G>A|p.Arg421His |
S188 |
| 51752 | BAA01g28610 | A01 | 17940435 | C | T | missense_variant | MODERATE | c.1310C>T|p.Ala437Val |
S166 |
| 51753 | BAA01g28610 | A01 | 17940602 | G | A | missense_variant | MODERATE | c.1477G>A|p.Glu493Lys |
S173 |
| 51754 | BAA01g28610 | A01 | 17940624 | C | T | missense_variant | MODERATE | c.1499C>T|p.Ser500Phe |
S68 |
| 51755 | BAA01g28610 | A01 | 17940974 | G | A | missense_variant | MODERATE | c.1849G>A|p.Gly617Ser |
S196 |
| 51756 | BAA01g28610 | A01 | 17940978 | C | T | missense_variant | MODERATE | c.1853C>T|p.Ser618Phe |
S39 |
| 51757 | BAA01g28610 | A01 | 17940985 | C | T | synonymous_variant | LOW | c.1860C>T|p.Phe620Phe |
S35 |
| 51758 | BAA01g28610 | A01 | 17941020 | C | T | missense_variant | MODERATE | c.1895C>T|p.Ser632Phe |
S219 S72 |
| 51759 | BAA01g28610 | A01 | 17942195 | C | T | downstream_gene_variant | MODIFIER | c.*167C>T| |
S114 S256 |
| 51760 | BAA01g28610 | A01 | 17942988 | G | A | downstream_gene_variant | MODIFIER | c.*960G>A| |
S283 |
| 51761 | BAA01g28610 | A01 | 17943196 | G | A | downstream_gene_variant | MODIFIER | c.*1168G>A| |
S38 |
| 51762 | BAA01g28610 | A01 | 17943241 | G | A | downstream_gene_variant | MODIFIER | c.*1213G>A| |
S306 S308 |
| 51763 | BAA01g28610 | A01 | 17943253 | G | A | downstream_gene_variant | MODIFIER | c.*1225G>A| |
S140 |
| 51764 | BAA01g28610 | A01 | 17943469 | C | T | downstream_gene_variant | MODIFIER | c.*1441C>T| |
S113 |
| 51765 | BAA01g28610 | A01 | 17943578 | G | A | downstream_gene_variant | MODIFIER | c.*1550G>A| |
S116 |
| 51766 | BAA01g28610 | A01 | 17943659 | C | T | downstream_gene_variant | MODIFIER | c.*1631C>T| |
S211 S227 |
| 51767 | BAA01g28610 | A01 | 17944091 | G | A | downstream_gene_variant | MODIFIER | c.*2063G>A| |
S33 |
| 51768 | BAA01g28640 | A01 | 17956049 | C | T | upstream_gene_variant | MODIFIER | c.-1302C>T| |
S43 |
| 51769 | BAA01g28650 | A01 | 17959490 | G | A | missense_variant | MODERATE | c.1195G>A|p.Val399Ile |
S67 |
| 51770 | BAA01g28670 | A01 | 17962361 | C | T | missense_variant | MODERATE | c.200G>A|p.Gly67Asp |
S242 |
| 51771 | BAA01g28670 | A01 | 17962609 | C | T | upstream_gene_variant | MODIFIER | c.-49G>A| |
S112 |
| 51772 | BAA01g28670 | A01 | 17962625 | C | T | upstream_gene_variant | MODIFIER | c.-65G>A| |
S184 |
| 51773 | BAA01g28670 | A01 | 17963222 | G | A | upstream_gene_variant | MODIFIER | c.-662C>T| |
S138 |
| 51774 | BAA01g28670 | A01 | 17963722 | C | T | upstream_gene_variant | MODIFIER | c.-1162G>A| |
S186 |
| 51775 | BAA01g28670 | A01 | 17963783 | C | T | upstream_gene_variant | MODIFIER | c.-1223G>A| |
S233 |