| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 168801 | BAA02g13980 | A02 | 6568903 | G | A | missense_variant | MODERATE | c.1082G>A|p.Arg361Lys |
S11 |
| 168802 | BAA02g13980 | A02 | 6569229 | G | A | missense_variant | MODERATE | c.1327G>A|p.Asp443Asn |
S279 |
| 168803 | BAA02g13980 | A02 | 6569929 | G | A | missense_variant | MODERATE | c.2027G>A|p.Gly676Glu |
S198 |
| 168804 | BAA02g13980 | A02 | 6569979 | C | T | missense_variant | MODERATE | c.2077C>T|p.Pro693Ser |
S308 |
| 168805 | BAA02g13980 | A02 | 6570656 | C | T | synonymous_variant | LOW | c.2754C>T|p.Ser918Ser |
S128 |
| 168806 | BAA02g13980 | A02 | 6572753 | G | A | downstream_gene_variant | MODIFIER | c.*1983G>A| |
S13 S168 S279 S64 |
| 168807 | BAA02g13980 | A02 | 6572798 | G | A | downstream_gene_variant | MODIFIER | c.*2028G>A| |
S23 |
| 168808 | BAA02g13990 | A02 | 6573578 | C | T | missense_variant | MODERATE | c.520G>A|p.Asp174Asn |
S25 |
| 168809 | BAA02g13990 | A02 | 6575503 | G | A | upstream_gene_variant | MODIFIER | c.-1406C>T| |
S41 |
| 168810 | BAA02g13990 | A02 | 6575519 | G | A | upstream_gene_variant | MODIFIER | c.-1422C>T| |
S272 |
| 168811 | BAA02g13990 | A02 | 6577111 | G | A | upstream_gene_variant | MODIFIER | c.-3014C>T| |
S231 |
| 168812 | BAA02g13990 | A02 | 6577124 | T | G | upstream_gene_variant | MODIFIER | c.-3027A>C| |
S171 S200 S282 S289 |
| 168813 | BAA02g13990 | A02 | 6577133 | G | A | upstream_gene_variant | MODIFIER | c.-3036C>T| |
S13 S157 S168 S279 S64 |
| 168814 | BAA02g14000 | A02 | 6579191 | G | A | downstream_gene_variant | MODIFIER | c.*2570C>T| |
S263 |
| 168815 | BAA02g14000 | A02 | 6579601 | G | A | downstream_gene_variant | MODIFIER | c.*2160C>T| |
S184 S80 |
| 168816 | BAA02g14000 | A02 | 6579790 | C | T | downstream_gene_variant | MODIFIER | c.*1971G>A| |
S40 |
| 168817 | BAA02g14010 | A02 | 6580575 | G | A | upstream_gene_variant | MODIFIER | c.-4700G>A| |
S173 |
| 168818 | BAA02g14010 | A02 | 6581713 | G | A | upstream_gene_variant | MODIFIER | c.-3562G>A| |
S246 |
| 168819 | BAA02g14000 | A02 | 6582021 | G | A | missense_variant | MODERATE | c.1066C>T|p.Leu356Phe |
S205 |
| 168820 | BAA02g14000 | A02 | 6582058 | C | T | synonymous_variant | LOW | c.1029G>A|p.Arg343Arg |
S206 S26 |
| 168821 | BAA02g14010 | A02 | 6582851 | C | T | upstream_gene_variant | MODIFIER | c.-2424C>T| |
S71 |
| 168822 | BAA02g14000 | A02 | 6584168 | C | T | upstream_gene_variant | MODIFIER | c.-211G>A| |
S33 |
| 168823 | BAA02g14000 | A02 | 6584359 | C | T | upstream_gene_variant | MODIFIER | c.-402G>A| |
S77 |
| 168824 | BAA02g14000 | A02 | 6584462 | C | T | upstream_gene_variant | MODIFIER | c.-505G>A| |
S116 |
| 168825 | BAA02g14010 | A02 | 6585440 | G | A | missense_variant | MODERATE | c.166G>A|p.Val56Met |
S59 |