Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g30130 | A01 | 19129132 | C | A | upstream_gene_variant | MODIFIER | c.-3138C>A| |
S239 |
2 | BAA01g30130 | A01 | 19130501 | G | A | upstream_gene_variant | MODIFIER | c.-1769G>A| |
S38 |
3 | BAA01g30130 | A01 | 19131795 | G | A | upstream_gene_variant | MODIFIER | c.-475G>A| |
S172 S217 |
4 | BAA01g30130 | A01 | 19131902 | C | T | upstream_gene_variant | MODIFIER | c.-368C>T| |
S107 |
5 | BAA01g30130 | A01 | 19132624 | C | T | missense_variant | MODERATE | c.194C>T|p.Thr65Ile |
S87 |
6 | BAA01g30130 | A01 | 19132961 | C | T | missense_variant | MODERATE | c.443C>T|p.Ser148Phe |
S282 |
7 | BAA01g30130 | A01 | 19133021 | G | A | missense_variant | MODERATE | c.503G>A|p.Arg168Lys |
S58 |
8 | BAA01g30130 | A01 | 19133222 | G | A | splice_region_variant&intron_variant | LOW | c.619-5G>A| |
S68 |
9 | BAA01g30130 | A01 | 19133474 | G | A | missense_variant | MODERATE | c.866G>A|p.Arg289Lys |
S161 |
10 | BAA01g30130 | A01 | 19134232 | C | T | intron_variant | MODIFIER | c.1269+195C>T| |
S132 S137 S215 S89 |
11 | BAA01g30130 | A01 | 19134267 | G | A | intron_variant | MODIFIER | c.1269+230G>A| |
S299 |
12 | BAA01g30130 | A01 | 19136099 | C | T | intron_variant | MODIFIER | c.1270-61C>T| |
S271 |
13 | BAA01g30130 | A01 | 19137578 | C | T | downstream_gene_variant | MODIFIER | c.*595C>T| |
S87 |
14 | BAA01g30130 | A01 | 19141218 | G | A | downstream_gene_variant | MODIFIER | c.*4235G>A| |
S298 |
15 | BAA01g30130 | A01 | 19141491 | C | T | downstream_gene_variant | MODIFIER | c.*4508C>T| |
S240 |