| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 185201 | BAA02g22960 | A02 | 12479061 | G | A | downstream_gene_variant | MODIFIER | c.*1825C>T| |
S239 |
| 185202 | BAA02g22950 | A02 | 12479180 | C | T | synonymous_variant | LOW | c.915C>T|p.Pro305Pro |
S118 |
| 185203 | BAA02g22950 | A02 | 12479872 | G | A | missense_variant | MODERATE | c.1189G>A|p.Glu397Lys |
S61 |
| 185204 | BAA02g22950 | A02 | 12479887 | G | A | missense_variant | MODERATE | c.1204G>A|p.Gly402Arg |
S230 |
| 185205 | BAA02g22970 | A02 | 12482390 | G | T | missense_variant | MODERATE | c.820C>A|p.Leu274Ile |
S301 S304 |
| 185206 | BAA02g22970 | A02 | 12482520 | C | T | synonymous_variant | LOW | c.690G>A|p.Glu230Glu |
S276 |
| 185207 | BAA02g22970 | A02 | 12482536 | G | A | missense_variant | MODERATE | c.674C>T|p.Pro225Leu |
S223 |
| 185208 | BAA02g22970 | A02 | 12482808 | G | A | synonymous_variant | LOW | c.402C>T|p.Asp134Asp |
S161 |
| 185209 | BAA02g22970 | A02 | 12482816 | G | A | missense_variant | MODERATE | c.394C>T|p.Leu132Phe |
S168 |
| 185210 | BAA02g22960 | A02 | 12483185 | G | A | upstream_gene_variant | MODIFIER | c.-1922C>T| |
S23 |
| 185211 | BAA02g22960 | A02 | 12483278 | C | T | upstream_gene_variant | MODIFIER | c.-2015G>A| |
S66 |
| 185212 | BAA02g22960 | A02 | 12484141 | G | A | upstream_gene_variant | MODIFIER | c.-2878C>T| |
S168 |
| 185213 | BAA02g22960 | A02 | 12484212 | G | A | upstream_gene_variant | MODIFIER | c.-2949C>T| |
S157 S33 |
| 185214 | BAA02g22960 | A02 | 12485464 | T | A | upstream_gene_variant | MODIFIER | c.-4201A>T| |
S163 |
| 185215 | BAA02g22960 | A02 | 12485922 | C | T | upstream_gene_variant | MODIFIER | c.-4659G>A| |
S86 |
| 185216 | BAA02g22970 | A02 | 12487053 | C | T | upstream_gene_variant | MODIFIER | c.-3191G>A| |
S25 |
| 185217 | BAA02g22970 | A02 | 12488205 | C | T | upstream_gene_variant | MODIFIER | c.-4343G>A| |
S175 |
| 185218 | BAA02g22970 | A02 | 12488740 | C | T | upstream_gene_variant | MODIFIER | c.-4878G>A| |
S305 |
| 185219 | BAA02g22980 | A02 | 12490470 | G | A | synonymous_variant | LOW | c.312C>T|p.Leu104Leu |
S132 S215 |
| 185220 | BAA02g22990 | A02 | 12490509 | C | T | upstream_gene_variant | MODIFIER | c.-1445C>T| |
S271 |
| 185221 | BAA02g22980 | A02 | 12490796 | C | T | splice_region_variant&intron_variant | LOW | c.193-6G>A| |
S276 |
| 185222 | BAA02g22990 | A02 | 12490951 | G | A | upstream_gene_variant | MODIFIER | c.-1003G>A| |
S92 |
| 185223 | BAA02g22980 | A02 | 12491140 | G | A | splice_region_variant&intron_variant | LOW | c.107+7C>T| |
S58 |
| 185224 | BAA02g23000 | A02 | 12493436 | G | A | missense_variant | MODERATE | c.1988C>T|p.Ala663Val |
S204 |
| 185225 | BAA02g22980 | A02 | 12494229 | C | T | upstream_gene_variant | MODIFIER | c.-2976G>A| |
S38 |