Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g03100 | A10 | 1507943 | C | T | missense_variant | MODERATE | c.2735G>A|p.Gly912Glu |
S166 |
2 | BAA10g03100 | A10 | 1508080 | C | T | synonymous_variant | LOW | c.2598G>A|p.Arg866Arg |
S249 |
3 | BAA10g03100 | A10 | 1509246 | G | A | missense_variant | MODERATE | c.2059C>T|p.Leu687Phe |
S71 |
4 | BAA10g03100 | A10 | 1509604 | G | A | synonymous_variant | LOW | c.1785C>T|p.Ala595Ala |
S115 |
5 | BAA10g03100 | A10 | 1510797 | C | T | synonymous_variant | LOW | c.690G>A|p.Gln230Gln |
S132 S137 S215 |
6 | BAA10g03100 | A10 | 1511465 | C | T | missense_variant | MODERATE | c.514G>A|p.Ala172Thr |
S200 |
7 | BAA10g03100 | A10 | 1511660 | C | T | missense_variant | MODERATE | c.319G>A|p.Val107Met |
S15 S156 S2 S3 S34 |
8 | BAA10g03100 | A10 | 1512425 | C | T | upstream_gene_variant | MODIFIER | c.-447G>A| |
S159 S187 S188 S243 S276 |
9 | BAA10g03100 | A10 | 1514229 | G | A | upstream_gene_variant | MODIFIER | c.-2251C>T| |
S198 |
10 | BAA10g03100 | A10 | 1516414 | G | A | upstream_gene_variant | MODIFIER | c.-4436C>T| |
S120 |