Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
5001 | BAA01g04080 | A01 | 1846053 | G | A | downstream_gene_variant | MODIFIER | c.*2799G>A| |
S236 |
5002 | BAA01g04090 | A01 | 1846089 | C | T | missense_variant | MODERATE | c.1106C>T|p.Ala369Val |
S182 S38 |
5003 | BAA01g04100 | A01 | 1847241 | C | T | missense_variant | MODERATE | c.2287G>A|p.Asp763Asn |
S144 |
5004 | BAA01g04100 | A01 | 1848232 | G | A | synonymous_variant | LOW | c.1677C>T|p.Ser559Ser |
S247 |
5005 | BAA01g04090 | A01 | 1848366 | C | T | downstream_gene_variant | MODIFIER | c.*2249C>T| |
S150 |
5006 | BAA01g04100 | A01 | 1848536 | G | A | splice_region_variant&intron_variant | LOW | c.1584+4C>T| |
S296 |
5007 | BAA01g04090 | A01 | 1849127 | G | A | downstream_gene_variant | MODIFIER | c.*3010G>A| |
S95 |
5008 | BAA01g04090 | A01 | 1849535 | G | T | downstream_gene_variant | MODIFIER | c.*3418G>T| |
S147 |
5009 | BAA01g04100 | A01 | 1849649 | G | A | synonymous_variant | LOW | c.946C>T|p.Leu316Leu |
S282 |
5010 | BAA01g04100 | A01 | 1850464 | C | T | missense_variant | MODERATE | c.478G>A|p.Ala160Thr |
S54 |
5011 | BAA01g04100 | A01 | 1851408 | G | A | upstream_gene_variant | MODIFIER | c.-56C>T| |
S217 |
5012 | BAA01g04110 | A01 | 1852675 | G | A | synonymous_variant | LOW | c.1437C>T|p.Tyr479Tyr |
S70 |
5013 | BAA01g04100 | A01 | 1852736 | G | A | upstream_gene_variant | MODIFIER | c.-1384C>T| |
S245 |
5014 | BAA01g04100 | A01 | 1853768 | C | T | upstream_gene_variant | MODIFIER | c.-2416G>A| |
S249 |
5015 | BAA01g04110 | A01 | 1854450 | G | A | missense_variant | MODERATE | c.272C>T|p.Ser91Phe |
S23 |
5016 | BAA01g04100 | A01 | 1854929 | G | A | upstream_gene_variant | MODIFIER | c.-3577C>T| |
S112 |
5017 | BAA01g04100 | A01 | 1855290 | G | A | upstream_gene_variant | MODIFIER | c.-3938C>T| |
S297 |
5018 | BAA01g04120 | A01 | 1856174 | G | A | missense_variant | MODERATE | c.2213C>T|p.Pro738Leu |
S156 |
5019 | BAA01g04120 | A01 | 1856323 | G | A | synonymous_variant | LOW | c.2064C>T|p.Leu688Leu |
S177 |
5020 | BAA01g04120 | A01 | 1859756 | C | T | upstream_gene_variant | MODIFIER | c.-825G>A| |
S168 |
5021 | BAA01g04130 | A01 | 1860256 | G | A | missense_variant | MODERATE | c.697C>T|p.Pro233Ser |
S251 |
5022 | BAA01g04120 | A01 | 1860611 | C | T | upstream_gene_variant | MODIFIER | c.-1680G>A| |
S100 |
5023 | BAA01g04120 | A01 | 1860624 | T | C | upstream_gene_variant | MODIFIER | c.-1693A>G| |
S291 |
5024 | BAA01g04120 | A01 | 1861366 | C | T | upstream_gene_variant | MODIFIER | c.-2435G>A| |
S130 |
5025 | BAA01g04120 | A01 | 1861529 | G | A | upstream_gene_variant | MODIFIER | c.-2598C>T| |
S251 |