| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 183251 | BAA02g21910 | A02 | 11804295 | C | T | upstream_gene_variant | MODIFIER | c.-4465G>A| |
S167 |
| 183252 | BAA02g21930 | A02 | 11804465 | C | T | missense_variant | MODERATE | c.250G>A|p.Gly84Ser |
S16 |
| 183253 | BAA02g21930 | A02 | 11805172 | C | T | upstream_gene_variant | MODIFIER | c.-367G>A| |
S240 S7 |
| 183254 | BAA02g21940 | A02 | 11805817 | G | A | missense_variant | MODERATE | c.73G>A|p.Glu25Lys |
S13 S140 S168 S279 S64 |
| 183255 | BAA02g21940 | A02 | 11805865 | G | A | missense_variant | MODERATE | c.121G>A|p.Gly41Arg |
S282 |
| 183256 | BAA02g21930 | A02 | 11806253 | G | A | upstream_gene_variant | MODIFIER | c.-1448C>T| |
S57 |
| 183257 | BAA02g21930 | A02 | 11807737 | T | C | upstream_gene_variant | MODIFIER | c.-2932A>G| |
S262 |
| 183258 | BAA02g21930 | A02 | 11807959 | C | T | upstream_gene_variant | MODIFIER | c.-3154G>A| |
S5 |
| 183259 | BAA02g21950 | A02 | 11808414 | G | A | missense_variant | MODERATE | c.13G>A|p.Glu5Lys |
S239 |
| 183260 | BAA02g21950 | A02 | 11809183 | G | A | synonymous_variant | LOW | c.510G>A|p.Arg170Arg |
S116 |
| 183261 | BAA02g21950 | A02 | 11809189 | C | T | synonymous_variant | LOW | c.516C>T|p.Phe172Phe |
S11 |
| 183262 | BAA02g21950 | A02 | 11809270 | G | A | synonymous_variant | LOW | c.597G>A|p.Leu199Leu |
S116 |
| 183263 | BAA02g21930 | A02 | 11809499 | G | A | upstream_gene_variant | MODIFIER | c.-4694C>T| |
S303 |
| 183264 | BAA02g21970 | A02 | 11811318 | C | T | upstream_gene_variant | MODIFIER | c.-4422C>T| |
S107 |
| 183265 | BAA02g21970 | A02 | 11811997 | G | A | upstream_gene_variant | MODIFIER | c.-3743G>A| |
S95 |
| 183266 | BAA02g21970 | A02 | 11812602 | G | A | upstream_gene_variant | MODIFIER | c.-3138G>A| |
S288 |
| 183267 | BAA02g21970 | A02 | 11813615 | C | T | upstream_gene_variant | MODIFIER | c.-2125C>T| |
S6 |
| 183268 | BAA02g21960 | A02 | 11813975 | C | T | missense_variant | MODERATE | c.1342G>A|p.Glu448Lys |
S2 |
| 183269 | BAA02g21960 | A02 | 11814037 | C | T | missense_variant | MODERATE | c.1280G>A|p.Arg427Gln |
S250 |
| 183270 | BAA02g21960 | A02 | 11814260 | C | T | missense_variant | MODERATE | c.1057G>A|p.Glu353Lys |
S284 |
| 183271 | BAA02g21960 | A02 | 11814366 | G | A | synonymous_variant | LOW | c.951C>T|p.Ile317Ile |
S156 |
| 183272 | BAA02g21960 | A02 | 11814764 | G | A | synonymous_variant | LOW | c.553C>T|p.Leu185Leu |
S129 |
| 183273 | BAA02g21960 | A02 | 11814802 | C | T | missense_variant | MODERATE | c.515G>A|p.Ser172Asn |
S80 |
| 183274 | BAA02g21960 | A02 | 11814807 | G | A | synonymous_variant | LOW | c.510C>T|p.Ser170Ser |
S50 |
| 183275 | BAA02g21960 | A02 | 11815057 | C | T | missense_variant | MODERATE | c.260G>A|p.Gly87Glu |
S305 |