| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 11001 | BAA01g08880 | A01 | 3920264 | G | A | upstream_gene_variant | MODIFIER | c.-4451C>T| |
S175 |
| 11002 | BAA01g08900 | A01 | 3920431 | G | A | synonymous_variant | LOW | c.156G>A|p.Lys52Lys |
S142 |
| 11003 | BAA01g08880 | A01 | 3920561 | G | A | upstream_gene_variant | MODIFIER | c.-4748C>T| |
S104 S52 |
| 11004 | BAA01g08930 | A01 | 3934016 | C | T | upstream_gene_variant | MODIFIER | c.-508G>A| |
S76 |
| 11005 | BAA01g08940 | A01 | 3934553 | C | T | missense_variant | MODERATE | c.136C>T|p.Leu46Phe |
S171 |
| 11006 | BAA01g08940 | A01 | 3934666 | C | T | synonymous_variant | LOW | c.249C>T|p.Thr83Thr |
S223 |
| 11007 | BAA01g08930 | A01 | 3935256 | C | T | upstream_gene_variant | MODIFIER | c.-1748G>A| |
S158 |
| 11008 | BAA01g08930 | A01 | 3935814 | C | T | upstream_gene_variant | MODIFIER | c.-2306G>A| |
S230 |
| 11009 | BAA01g08930 | A01 | 3936103 | C | T | upstream_gene_variant | MODIFIER | c.-2595G>A| |
S263 |
| 11010 | BAA01g08960 | A01 | 3937534 | G | A | missense_variant | MODERATE | c.205G>A|p.Glu69Lys |
S123 |
| 11011 | BAA01g08960 | A01 | 3938265 | C | T | synonymous_variant | LOW | c.936C>T|p.Ser312Ser |
S256 |
| 11012 | BAA01g08960 | A01 | 3938557 | G | A | missense_variant | MODERATE | c.1162G>A|p.Val388Ile |
S124 |
| 11013 | BAA01g08970 | A01 | 3938933 | G | A | upstream_gene_variant | MODIFIER | c.-2388G>A| |
S245 |
| 11014 | BAA01g08960 | A01 | 3939893 | G | A | missense_variant | MODERATE | c.2089G>A|p.Asp697Asn |
S70 |
| 11015 | BAA01g08960 | A01 | 3939910 | G | A | synonymous_variant | LOW | c.2106G>A|p.Lys702Lys |
S27 |
| 11016 | BAA01g08970 | A01 | 3940273 | G | A | upstream_gene_variant | MODIFIER | c.-1048G>A| |
S104 S52 |
| 11017 | BAA01g08970 | A01 | 3942185 | C | T | synonymous_variant | LOW | c.414C>T|p.Pro138Pro |
S226 S45 |
| 11018 | BAA01g08980 | A01 | 3942291 | C | T | upstream_gene_variant | MODIFIER | c.-4498C>T| |
S241 |
| 11019 | BAA01g08970 | A01 | 3942629 | C | T | missense_variant | MODERATE | c.617C>T|p.Thr206Ile |
S249 |
| 11020 | BAA01g08980 | A01 | 3943531 | G | A | upstream_gene_variant | MODIFIER | c.-3258G>A| |
S294 |
| 11021 | BAA01g08980 | A01 | 3944190 | C | T | upstream_gene_variant | MODIFIER | c.-2599C>T| |
S206 S26 |
| 11022 | BAA01g08980 | A01 | 3944724 | C | T | upstream_gene_variant | MODIFIER | c.-2065C>T| |
S36 |
| 11023 | BAA01g08980 | A01 | 3945753 | C | T | upstream_gene_variant | MODIFIER | c.-1036C>T| |
S286 |
| 11024 | BAA01g08980 | A01 | 3946069 | G | A | upstream_gene_variant | MODIFIER | c.-720G>A| |
S274 |
| 11025 | BAA01g08980 | A01 | 3946200 | G | A | upstream_gene_variant | MODIFIER | c.-589G>A| |
S104 S105 S52 |