Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39340 | A01 | 26115733 | C | T | downstream_gene_variant | MODIFIER | c.*2424G>A| |
S18 |
2 | BAA01g39340 | A01 | 26115835 | C | T | downstream_gene_variant | MODIFIER | c.*2322G>A| |
S303 |
3 | BAA01g39340 | A01 | 26118168 | C | T | missense_variant | MODERATE | c.841G>A|p.Ala281Thr |
S294 |
4 | BAA01g39340 | A01 | 26118333 | G | A | missense_variant | MODERATE | c.676C>T|p.Leu226Phe |
S84 S93 |
5 | BAA01g39340 | A01 | 26118389 | C | T | missense_variant | MODERATE | c.620G>A|p.Arg207Lys |
S233 |
6 | BAA01g39340 | A01 | 26120400 | G | A | synonymous_variant | LOW | c.457C>T|p.Leu153Leu |
S125 |
7 | BAA01g39340 | A01 | 26122986 | G | A | intron_variant | MODIFIER | c.263-2392C>T| |
S15 |
8 | BAA01g39340 | A01 | 26124155 | C | T | intron_variant | MODIFIER | c.262+3185G>A| |
S89 |
9 | BAA01g39340 | A01 | 26124198 | C | T | intron_variant | MODIFIER | c.262+3142G>A| |
S39 |
10 | BAA01g39340 | A01 | 26124316 | G | A | intron_variant | MODIFIER | c.262+3024C>T| |
S122 |
11 | BAA01g39340 | A01 | 26124818 | G | A | intron_variant | MODIFIER | c.262+2522C>T| |
S152 |
12 | BAA01g39340 | A01 | 26124876 | C | T | intron_variant | MODIFIER | c.262+2464G>A| |
S256 |
13 | BAA01g39340 | A01 | 26125335 | G | A | intron_variant | MODIFIER | c.262+2005C>T| |
S2 |
14 | BAA01g39340 | A01 | 26126309 | C | T | intron_variant | MODIFIER | c.262+1031G>A| |
S18 |
15 | BAA01g39340 | A01 | 26130334 | C | T | upstream_gene_variant | MODIFIER | c.-2733G>A| |
S77 S82 |
16 | BAA01g39340 | A01 | 26132180 | G | A | upstream_gene_variant | MODIFIER | c.-4579C>T| |
S224 |
17 | BAA01g39340 | A01 | 26132441 | G | A | upstream_gene_variant | MODIFIER | c.-4840C>T| |
S117 |