Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g45560 | A02 | 37259483 | G | A | downstream_gene_variant | MODIFIER | c.*4860C>T| |
S278 |
2 | BAA02g45560 | A02 | 37260422 | C | T | downstream_gene_variant | MODIFIER | c.*3921G>A| |
S42 |
3 | BAA02g45560 | A02 | 37261145 | G | A | downstream_gene_variant | MODIFIER | c.*3198C>T| |
S283 |
4 | BAA02g45560 | A02 | 37262227 | C | T | downstream_gene_variant | MODIFIER | c.*2116G>A| |
S144 |
5 | BAA02g45560 | A02 | 37264401 | G | A | missense_variant | MODERATE | c.2324C>T|p.Ala775Val |
S292 |
6 | BAA02g45560 | A02 | 37265046 | C | T | missense_variant | MODERATE | c.1954G>A|p.Gly652Arg |
S182 |
7 | BAA02g45560 | A02 | 37265189 | G | A | missense_variant | MODERATE | c.1811C>T|p.Ser604Phe |
S268 |
8 | BAA02g45560 | A02 | 37265321 | C | T | missense_variant | MODERATE | c.1679G>A|p.Ser560Asn |
S48 |
9 | BAA02g45560 | A02 | 37266078 | C | T | missense_variant | MODERATE | c.922G>A|p.Asp308Asn |
S295 |
10 | BAA02g45560 | A02 | 37267170 | C | T | synonymous_variant | LOW | c.846G>A|p.Glu282Glu |
S249 |
11 | BAA02g45560 | A02 | 37267178 | C | T | missense_variant | MODERATE | c.838G>A|p.Glu280Lys |
S92 |
12 | BAA02g45560 | A02 | 37268424 | C | T | synonymous_variant | LOW | c.411G>A|p.Val137Val |
S167 |
13 | BAA02g45560 | A02 | 37268695 | C | T | missense_variant | MODERATE | c.140G>A|p.Arg47Lys |
S189 |
14 | BAA02g45560 | A02 | 37269446 | C | T | upstream_gene_variant | MODIFIER | c.-158G>A| |
S15 |
15 | BAA02g45560 | A02 | 37270593 | C | T | upstream_gene_variant | MODIFIER | c.-1305G>A| |
S167 |
16 | BAA02g45560 | A02 | 37270786 | G | A | upstream_gene_variant | MODIFIER | c.-1498C>T| |
S114 |