Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g27190 | A10 | 21276750 | C | T | upstream_gene_variant | MODIFIER | c.-4129C>T| |
S161 |
2 | BAA10g27190 | A10 | 21277118 | C | T | upstream_gene_variant | MODIFIER | c.-3761C>T| |
S272 |
3 | BAA10g27190 | A10 | 21279782 | G | A | upstream_gene_variant | MODIFIER | c.-1097G>A| |
S62 |
4 | BAA10g27190 | A10 | 21279876 | C | T | upstream_gene_variant | MODIFIER | c.-1003C>T| |
S203 |
5 | BAA10g27190 | A10 | 21280117 | C | T | upstream_gene_variant | MODIFIER | c.-762C>T| |
S306 S308 |
6 | BAA10g27190 | A10 | 21280633 | C | T | upstream_gene_variant | MODIFIER | c.-246C>T| |
S247 |
7 | BAA10g27190 | A10 | 21281508 | G | A | intron_variant | MODIFIER | c.303+233G>A| |
S274 |
8 | BAA10g27190 | A10 | 21281745 | C | T | intron_variant | MODIFIER | c.303+470C>T| |
S68 |
9 | BAA10g27190 | A10 | 21283231 | G | A | missense_variant | MODERATE | c.520G>A|p.Glu174Lys |
S131 |
10 | BAA10g27190 | A10 | 21283307 | A | G | missense_variant | MODERATE | c.596A>G|p.Gln199Arg |
S103 |
11 | BAA10g27190 | A10 | 21283927 | G | A | synonymous_variant | LOW | c.852G>A|p.Leu284Leu |
S139 |