Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10260 | A10 | 12023828 | G | A | missense_variant | MODERATE | c.995C>T|p.Thr332Met |
S217 S248 |
2 | BAA10g10260 | A10 | 12023900 | C | T | missense_variant | MODERATE | c.923G>A|p.Gly308Glu |
S38 |
3 | BAA10g10260 | A10 | 12023955 | C | T | missense_variant | MODERATE | c.868G>A|p.Val290Met |
S249 |
4 | BAA10g10260 | A10 | 12025232 | G | A | missense_variant | MODERATE | c.239C>T|p.Thr80Ile |
S216 |
5 | BAA10g10260 | A10 | 12026352 | G | A | upstream_gene_variant | MODIFIER | c.-810C>T| |
S127 |
6 | BAA10g10260 | A10 | 12026945 | G | A | upstream_gene_variant | MODIFIER | c.-1403C>T| |
S293 |
7 | BAA10g10260 | A10 | 12027481 | G | A | upstream_gene_variant | MODIFIER | c.-1939C>T| |
S69 |
8 | BAA10g10260 | A10 | 12028202 | C | T | upstream_gene_variant | MODIFIER | c.-2660G>A| |
S195 |
9 | BAA10g10260 | A10 | 12028218 | C | T | upstream_gene_variant | MODIFIER | c.-2676G>A| |
S168 S70 |
10 | BAA10g10260 | A10 | 12028233 | G | A | upstream_gene_variant | MODIFIER | c.-2691C>T| |
S53 |
11 | BAA10g10260 | A10 | 12029311 | C | T | upstream_gene_variant | MODIFIER | c.-3769G>A| |
S79 S91 |