Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g04100 | A01 | 1847241 | C | T | missense_variant | MODERATE | c.2287G>A|p.Asp763Asn |
S144 |
2 | BAA01g04100 | A01 | 1848232 | G | A | synonymous_variant | LOW | c.1677C>T|p.Ser559Ser |
S247 |
3 | BAA01g04100 | A01 | 1848536 | G | A | splice_region_variant&intron_variant | LOW | c.1584+4C>T| |
S296 |
4 | BAA01g04100 | A01 | 1849649 | G | A | synonymous_variant | LOW | c.946C>T|p.Leu316Leu |
S282 |
5 | BAA01g04100 | A01 | 1850464 | C | T | missense_variant | MODERATE | c.478G>A|p.Ala160Thr |
S54 |
6 | BAA01g04100 | A01 | 1851408 | G | A | upstream_gene_variant | MODIFIER | c.-56C>T| |
S217 |
7 | BAA01g04100 | A01 | 1852736 | G | A | upstream_gene_variant | MODIFIER | c.-1384C>T| |
S245 |
8 | BAA01g04100 | A01 | 1853768 | C | T | upstream_gene_variant | MODIFIER | c.-2416G>A| |
S249 |
9 | BAA01g04100 | A01 | 1854929 | G | A | upstream_gene_variant | MODIFIER | c.-3577C>T| |
S112 |
10 | BAA01g04100 | A01 | 1855290 | G | A | upstream_gene_variant | MODIFIER | c.-3938C>T| |
S297 |