| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 184951 | BAA02g22850 | A02 | 12392749 | C | T | downstream_gene_variant | MODIFIER | c.*1419C>T| |
S299 |
| 184952 | BAA02g22860 | A02 | 12394347 | G | A | upstream_gene_variant | MODIFIER | c.-3926G>A| |
S298 |
| 184953 | BAA02g22860 | A02 | 12394821 | G | A | upstream_gene_variant | MODIFIER | c.-3452G>A| |
S125 |
| 184954 | BAA02g22860 | A02 | 12394921 | G | A | upstream_gene_variant | MODIFIER | c.-3352G>A| |
S28 |
| 184955 | BAA02g22860 | A02 | 12396165 | C | T | upstream_gene_variant | MODIFIER | c.-2108C>T| |
S183 S198 |
| 184956 | BAA02g22860 | A02 | 12396508 | C | T | upstream_gene_variant | MODIFIER | c.-1765C>T| |
S171 |
| 184957 | BAA02g22860 | A02 | 12396939 | C | T | upstream_gene_variant | MODIFIER | c.-1334C>T| |
S49 |
| 184958 | BAA02g22860 | A02 | 12398420 | G | A | missense_variant | MODERATE | c.148G>A|p.Glu50Lys |
S288 |
| 184959 | BAA02g22860 | A02 | 12398819 | G | A | downstream_gene_variant | MODIFIER | c.*46G>A| |
S45 |
| 184960 | BAA02g22860 | A02 | 12400206 | G | A | downstream_gene_variant | MODIFIER | c.*1433G>A| |
S259 |
| 184961 | BAA02g22860 | A02 | 12400943 | C | T | downstream_gene_variant | MODIFIER | c.*2170C>T| |
S99 |
| 184962 | BAA02g22860 | A02 | 12401316 | C | T | downstream_gene_variant | MODIFIER | c.*2543C>T| |
S135 S6 |
| 184963 | BAA02g22860 | A02 | 12402296 | G | A | downstream_gene_variant | MODIFIER | c.*3523G>A| |
S231 |
| 184964 | BAA02g22860 | A02 | 12402947 | C | T | downstream_gene_variant | MODIFIER | c.*4174C>T| |
S84 S93 |
| 184965 | BAA02g22870 | A02 | 12403472 | C | T | upstream_gene_variant | MODIFIER | c.-4754C>T| |
S56 |
| 184966 | BAA02g22870 | A02 | 12403495 | C | T | upstream_gene_variant | MODIFIER | c.-4731C>T| |
S53 |
| 184967 | BAA02g22870 | A02 | 12403721 | C | T | upstream_gene_variant | MODIFIER | c.-4505C>T| |
S201 |
| 184968 | BAA02g22870 | A02 | 12405277 | G | A | upstream_gene_variant | MODIFIER | c.-2949G>A| |
S139 |
| 184969 | BAA02g22870 | A02 | 12406257 | G | A | upstream_gene_variant | MODIFIER | c.-1969G>A| |
S58 |
| 184970 | BAA02g22870 | A02 | 12406959 | G | A | upstream_gene_variant | MODIFIER | c.-1267G>A| |
S162 |
| 184971 | BAA02g22870 | A02 | 12407220 | C | T | upstream_gene_variant | MODIFIER | c.-1006C>T| |
S216 |
| 184972 | BAA02g22870 | A02 | 12408021 | G | A | upstream_gene_variant | MODIFIER | c.-205G>A| |
S48 |
| 184973 | BAA02g22870 | A02 | 12408290 | C | T | missense_variant | MODERATE | c.65C>T|p.Ser22Phe |
S267 |
| 184974 | BAA02g22870 | A02 | 12408405 | G | A | synonymous_variant | LOW | c.180G>A|p.Ala60Ala |
S47 |
| 184975 | BAA02g22870 | A02 | 12408452 | G | A | missense_variant | MODERATE | c.227G>A|p.Gly76Asp |
S188 |