| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 15001 | BAA01g11610 | A01 | 5371506 | G | A | upstream_gene_variant | MODIFIER | c.-832C>T| |
S271 |
| 15002 | BAA01g11620 | A01 | 5371851 | C | T | missense_variant | MODERATE | c.166C>T|p.Pro56Ser |
S61 |
| 15003 | BAA01g11620 | A01 | 5372049 | C | T | missense_variant | MODERATE | c.281C>T|p.Ala94Val |
S203 |
| 15004 | BAA01g11620 | A01 | 5372356 | G | A | splice_region_variant&synonymous_variant | LOW | c.519G>A|p.Gln173Gln |
S129 |
| 15005 | BAA01g11620 | A01 | 5372698 | C | T | synonymous_variant | LOW | c.795C>T|p.Ile265Ile |
S206 S26 |
| 15006 | BAA01g11610 | A01 | 5373215 | C | T | upstream_gene_variant | MODIFIER | c.-2541G>A| |
S48 |
| 15007 | BAA01g11610 | A01 | 5374084 | C | T | upstream_gene_variant | MODIFIER | c.-3410G>A| |
S120 |
| 15008 | BAA01g11630 | A01 | 5375023 | C | T | missense_variant | MODERATE | c.304C>T|p.Pro102Ser |
S47 |
| 15009 | BAA01g11630 | A01 | 5375664 | C | T | missense_variant | MODERATE | c.784C>T|p.Leu262Phe |
S50 |
| 15010 | BAA01g11630 | A01 | 5376429 | C | T | missense_variant | MODERATE | c.1315C>T|p.Arg439Trp |
S144 |
| 15011 | BAA01g11620 | A01 | 5377241 | C | T | downstream_gene_variant | MODIFIER | c.*4465C>T| |
S196 |
| 15012 | BAA01g11620 | A01 | 5377282 | G | A | downstream_gene_variant | MODIFIER | c.*4506G>A| |
S262 |
| 15013 | BAA01g11630 | A01 | 5377869 | C | T | downstream_gene_variant | MODIFIER | c.*783C>T| |
S305 |
| 15014 | BAA01g11630 | A01 | 5377889 | G | A | downstream_gene_variant | MODIFIER | c.*803G>A| |
S3 |
| 15015 | BAA01g11630 | A01 | 5378131 | C | T | downstream_gene_variant | MODIFIER | c.*1045C>T| |
S100 |
| 15016 | BAA01g11630 | A01 | 5379427 | G | A | downstream_gene_variant | MODIFIER | c.*2341G>A| |
S195 |
| 15017 | BAA01g11630 | A01 | 5379637 | C | T | downstream_gene_variant | MODIFIER | c.*2551C>T| |
S202 |
| 15018 | BAA01g11630 | A01 | 5379651 | C | T | downstream_gene_variant | MODIFIER | c.*2565C>T| |
S295 |
| 15019 | BAA01g11630 | A01 | 5379673 | C | T | downstream_gene_variant | MODIFIER | c.*2587C>T| |
S118 |
| 15020 | BAA01g11630 | A01 | 5379919 | C | T | downstream_gene_variant | MODIFIER | c.*2833C>T| |
S278 |
| 15021 | BAA01g11630-BAA01g11640 | A01 | 5387232 | G | A | intergenic_region | MODIFIER | n.5387232G>A| |
S188 |
| 15022 | BAA01g11640 | A01 | 5387906 | C | T | upstream_gene_variant | MODIFIER | c.-4717C>T| |
S70 |
| 15023 | BAA01g11640 | A01 | 5389994 | C | T | upstream_gene_variant | MODIFIER | c.-2629C>T| |
S164 |
| 15024 | BAA01g11640 | A01 | 5392725 | C | A | missense_variant | MODERATE | c.103C>A|p.Pro35Thr |
S249 |
| 15025 | BAA01g11640 | A01 | 5392799 | C | T | synonymous_variant | LOW | c.177C>T|p.Val59Val |
S53 |