| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 161701 | BAA02g08760 | A02 | 3872305 | G | A | missense_variant | MODERATE | c.458C>T|p.Ser153Phe |
S189 |
| 161702 | BAA02g08760 | A02 | 3872906 | A | G | missense_variant | MODERATE | c.413T>C|p.Phe138Ser |
S25 |
| 161703 | BAA02g08760 | A02 | 3872928 | G | A | missense_variant | MODERATE | c.391C>T|p.Pro131Ser |
S28 |
| 161704 | BAA02g08760 | A02 | 3873156 | G | A | missense_variant | MODERATE | c.163C>T|p.Pro55Ser |
S19 |
| 161705 | BAA02g08760 | A02 | 3875880 | C | T | upstream_gene_variant | MODIFIER | c.-2562G>A| |
S277 |
| 161706 | BAA02g08760 | A02 | 3876161 | G | A | upstream_gene_variant | MODIFIER | c.-2843C>T| |
S105 S106 |
| 161707 | BAA02g08760 | A02 | 3877077 | G | A | upstream_gene_variant | MODIFIER | c.-3759C>T| |
S98 |
| 161708 | BAA02g08760 | A02 | 3877180 | C | T | upstream_gene_variant | MODIFIER | c.-3862G>A| |
S38 |
| 161709 | BAA02g08770 | A02 | 3878262 | G | A | missense_variant | MODERATE | c.311G>A|p.Arg104Lys |
S79 S91 |
| 161710 | BAA02g08770 | A02 | 3878706 | G | A | missense_variant | MODERATE | c.553G>A|p.Ala185Thr |
S97 |
| 161711 | BAA02g08770 | A02 | 3878896 | G | A | missense_variant&splice_region_variant | MODERATE | c.655G>A|p.Gly219Arg |
S266 |
| 161712 | BAA02g08770 | A02 | 3879229 | C | T | intron_variant | MODIFIER | c.781+17C>T| |
S195 |
| 161713 | BAA02g08770 | A02 | 3879908 | C | T | missense_variant | MODERATE | c.1175C>T|p.Pro392Leu |
S104 |
| 161714 | BAA02g08770 | A02 | 3880013 | G | A | missense_variant | MODERATE | c.1280G>A|p.Ser427Asn |
S84 S93 |
| 161715 | BAA02g08770 | A02 | 3880016 | G | A | missense_variant | MODERATE | c.1283G>A|p.Gly428Glu |
S209 |
| 161716 | BAA02g08770 | A02 | 3881010 | C | T | missense_variant | MODERATE | c.1700C>T|p.Ser567Phe |
S78 |
| 161717 | BAA02g08770 | A02 | 3881573 | C | T | missense_variant | MODERATE | c.1942C>T|p.His648Tyr |
S167 |
| 161718 | BAA02g08770 | A02 | 3881719 | G | A | missense_variant | MODERATE | c.2005G>A|p.Glu669Lys |
S204 |
| 161719 | BAA02g08770 | A02 | 3881755 | G | A | missense_variant | MODERATE | c.2041G>A|p.Glu681Lys |
S37 |
| 161720 | BAA02g08770 | A02 | 3882234 | C | T | synonymous_variant | LOW | c.2355C>T|p.Pro785Pro |
S263 |
| 161721 | BAA02g08770 | A02 | 3882481 | G | A | missense_variant | MODERATE | c.2398G>A|p.Glu800Lys |
S139 |
| 161722 | BAA02g08770 | A02 | 3885575 | C | T | downstream_gene_variant | MODIFIER | c.*2903C>T| |
S16 |
| 161723 | BAA02g08780 | A02 | 3886247 | G | A | missense_variant | MODERATE | c.1291G>A|p.Glu431Lys |
S163 |
| 161724 | BAA02g08780 | A02 | 3886346 | G | A | missense_variant | MODERATE | c.1390G>A|p.Gly464Arg |
S282 |
| 161725 | BAA02g08780 | A02 | 3886749 | C | T | missense_variant | MODERATE | c.1793C>T|p.Pro598Leu |
S23 |