Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03490 | A10 | 1689733 | C | T | synonymous_variant | LOW | c.597G>A|p.Arg199Arg |
S233 |
2 | BAA10g03490 | A10 | 1689999 | C | T | missense_variant | MODERATE | c.331G>A|p.Ala111Thr |
S173 |
3 | BAA10g03490 | A10 | 1690885 | G | A | upstream_gene_variant | MODIFIER | c.-556C>T| |
S161 |
4 | BAA10g03490 | A10 | 1692362 | G | A | upstream_gene_variant | MODIFIER | c.-2033C>T| |
S209 |
5 | BAA10g03490 | A10 | 1692371 | C | T | upstream_gene_variant | MODIFIER | c.-2042G>A| |
S116 |
6 | BAA10g03490 | A10 | 1692472 | G | A | upstream_gene_variant | MODIFIER | c.-2143C>T| |
S19 |
7 | BAA10g03490 | A10 | 1692534 | G | A | upstream_gene_variant | MODIFIER | c.-2205C>T| |
S268 |
8 | BAA10g03490 | A10 | 1693085 | G | A | upstream_gene_variant | MODIFIER | c.-2756C>T| |
S284 |
9 | BAA10g03490 | A10 | 1695014 | C | T | upstream_gene_variant | MODIFIER | c.-4685G>A| |
S162 |
10 | BAA10g03490 | A10 | 1695074 | C | T | upstream_gene_variant | MODIFIER | c.-4745G>A| |
S42 |
11 | BAA10g03490 | A10 | 1695293 | G | A | upstream_gene_variant | MODIFIER | c.-4964C>T| |
S178 |