Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g20260 | A07 | 25589367 | G | A | upstream_gene_variant | MODIFIER | c.-2670G>A| |
S54 |
2 | BAA07g20260 | A07 | 25589592 | C | T | upstream_gene_variant | MODIFIER | c.-2445C>T| |
S262 |
3 | BAA07g20260 | A07 | 25590733 | C | T | upstream_gene_variant | MODIFIER | c.-1304C>T| |
S162 |
4 | BAA07g20260 | A07 | 25591819 | G | A | upstream_gene_variant | MODIFIER | c.-218G>A| |
S199 |
5 | BAA07g20260 | A07 | 25592202 | G | A | missense_variant | MODERATE | c.166G>A|p.Gly56Arg |
S110 |
6 | BAA07g20260 | A07 | 25593572 | G | A | synonymous_variant | LOW | c.534G>A|p.Arg178Arg |
S219 S72 |
7 | BAA07g20260 | A07 | 25594020 | G | A | missense_variant | MODERATE | c.982G>A|p.Ala328Thr |
S105 |
8 | BAA07g20260 | A07 | 25594068 | G | A | missense_variant | MODERATE | c.1030G>A|p.Ala344Thr |
S171 |
9 | BAA07g20260 | A07 | 25594236 | G | A | missense_variant | MODERATE | c.1198G>A|p.Ala400Thr |
S202 |
10 | BAA07g20260 | A07 | 25594237 | C | T | missense_variant | MODERATE | c.1199C>T|p.Ala400Val |
S8 |