Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21090 | A10 | 18675011 | C | T | missense_variant | MODERATE | c.2924G>A|p.Gly975Glu |
S48 |
2 | BAA10g21090 | A10 | 18675398 | G | A | missense_variant | MODERATE | c.2537C>T|p.Ser846Phe |
S243 S299 |
3 | BAA10g21090 | A10 | 18676910 | G | A | missense_variant | MODERATE | c.1025C>T|p.Thr342Ile |
S293 |
4 | BAA10g21090 | A10 | 18677155 | C | T | missense_variant | MODERATE | c.860G>A|p.Gly287Asp |
S11 |
5 | BAA10g21090 | A10 | 18677419 | C | T | synonymous_variant | LOW | c.708G>A|p.Glu236Glu |
S122 |
6 | BAA10g21090 | A10 | 18678374 | G | A | missense_variant | MODERATE | c.35C>T|p.Ser12Phe |
S79 S84 |
7 | BAA10g21090 | A10 | 18678536 | G | A | upstream_gene_variant | MODIFIER | c.-128C>T| |
S175 S293 |
8 | BAA10g21090 | A10 | 18678809 | C | T | upstream_gene_variant | MODIFIER | c.-401G>A| |
S244 |
9 | BAA10g21090 | A10 | 18680684 | G | A | upstream_gene_variant | MODIFIER | c.-2276C>T| |
S28 |
10 | BAA10g21090 | A10 | 18681139 | C | T | upstream_gene_variant | MODIFIER | c.-2731G>A| |
S41 |