Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g25800 | A10 | 20699022 | G | A | missense_variant | MODERATE | c.1555C>T|p.Leu519Phe |
S81 S85 |
2 | BAA10g25800 | A10 | 20699230 | G | A | synonymous_variant | LOW | c.1347C>T|p.Ile449Ile |
S9 |
3 | BAA10g25800 | A10 | 20699247 | G | A | synonymous_variant | LOW | c.1330C>T|p.Leu444Leu |
S158 |
4 | BAA10g25800 | A10 | 20699671 | G | A | synonymous_variant | LOW | c.906C>T|p.Leu302Leu |
S160 |
5 | BAA10g25800 | A10 | 20700002 | C | T | missense_variant | MODERATE | c.575G>A|p.Arg192His |
S18 |
6 | BAA10g25800 | A10 | 20701449 | C | T | upstream_gene_variant | MODIFIER | c.-873G>A| |
S16 |
7 | BAA10g25800 | A10 | 20701622 | C | T | upstream_gene_variant | MODIFIER | c.-1046G>A| |
S14 |
8 | BAA10g25800 | A10 | 20701813 | C | T | upstream_gene_variant | MODIFIER | c.-1237G>A| |
S157 |
9 | BAA10g25800 | A10 | 20701902 | C | A | upstream_gene_variant | MODIFIER | c.-1326G>T| |
S5 |
10 | BAA10g25800 | A10 | 20701903 | G | A | upstream_gene_variant | MODIFIER | c.-1327C>T| |
S159 S243 |
11 | BAA10g25800 | A10 | 20702027 | G | A | upstream_gene_variant | MODIFIER | c.-1451C>T| |
S261 |
12 | BAA10g25800 | A10 | 20702036 | G | A | upstream_gene_variant | MODIFIER | c.-1460C>T| |
S262 |
13 | BAA10g25800 | A10 | 20702211 | G | A | upstream_gene_variant | MODIFIER | c.-1635C>T| |
S273 |
14 | BAA10g25800 | A10 | 20703443 | C | T | upstream_gene_variant | MODIFIER | c.-2867G>A| |
S23 |
15 | BAA10g25800 | A10 | 20704816 | C | T | upstream_gene_variant | MODIFIER | c.-4240G>A| |
S260 |