Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g12550 | A07 | 20829481 | C | T | upstream_gene_variant | MODIFIER | c.-2344C>T| |
S189 |
2 | BAA07g12550 | A07 | 20829849 | C | T | upstream_gene_variant | MODIFIER | c.-1976C>T| |
S142 |
3 | BAA07g12550 | A07 | 20830688 | G | A | upstream_gene_variant | MODIFIER | c.-1137G>A| |
S292 |
4 | BAA07g12550 | A07 | 20831263 | C | T | upstream_gene_variant | MODIFIER | c.-562C>T| |
S204 |
5 | BAA07g12550 | A07 | 20832256 | G | A | intron_variant | MODIFIER | c.390+42G>A| |
S132 S89 |
6 | BAA07g12550 | A07 | 20832270 | G | A | intron_variant | MODIFIER | c.390+56G>A| |
S223 |
7 | BAA07g12550 | A07 | 20832478 | G | A | intron_variant | MODIFIER | c.391-92G>A| |
S94 |
8 | BAA07g12550 | A07 | 20834317 | G | A | missense_variant | MODERATE | c.1999G>A|p.Ala667Thr |
S53 |
9 | BAA07g12550 | A07 | 20834759 | C | T | missense_variant | MODERATE | c.2258C>T|p.Ser753Phe |
S301 S304 |
10 | BAA07g12550 | A07 | 20835193 | G | A | missense_variant | MODERATE | c.2321G>A|p.Gly774Glu |
S134 |
11 | BAA07g12550 | A07 | 20836131 | G | A | stop_gained | HIGH | c.2958G>A|p.Trp986* |
S238 |