Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07850 | A10 | 4911376 | G | A | missense_variant | MODERATE | c.943C>T|p.Pro315Ser |
S64 |
2 | BAA10g07850 | A10 | 4911545 | C | T | synonymous_variant | LOW | c.774G>A|p.Thr258Thr |
S200 |
3 | BAA10g07850 | A10 | 4911559 | G | A | missense_variant | MODERATE | c.760C>T|p.Leu254Phe |
S69 |
4 | BAA10g07850 | A10 | 4911963 | G | A | missense_variant | MODERATE | c.434C>T|p.Ser145Leu |
S148 S210 S30 S31 |
5 | BAA10g07850 | A10 | 4912448 | G | A | synonymous_variant | LOW | c.48C>T|p.Phe16Phe |
S217 S248 |
6 | BAA10g07850 | A10 | 4912481 | C | T | synonymous_variant | LOW | c.15G>A|p.Gly5Gly |
S210 S225 |
7 | BAA10g07850 | A10 | 4912503 | G | A | upstream_gene_variant | MODIFIER | c.-8C>T| |
S172 S217 |
8 | BAA10g07850 | A10 | 4912518 | G | A | upstream_gene_variant | MODIFIER | c.-23C>T| |
S280 |
9 | BAA10g07850 | A10 | 4912666 | G | A | upstream_gene_variant | MODIFIER | c.-171C>T| |
S306 |
10 | BAA10g07850 | A10 | 4912829 | G | A | upstream_gene_variant | MODIFIER | c.-334C>T| |
S161 |
11 | BAA10g07850 | A10 | 4914016 | G | A | upstream_gene_variant | MODIFIER | c.-1521C>T| |
S1 |
12 | BAA10g07850 | A10 | 4917407 | G | A | upstream_gene_variant | MODIFIER | c.-4912C>T| |
S181 |