Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g01590 | A10 | 769075 | G | A | upstream_gene_variant | MODIFIER | c.-4332G>A| |
S289 |
2 | BAA10g01590 | A10 | 769148 | C | T | upstream_gene_variant | MODIFIER | c.-4259C>T| |
S202 |
3 | BAA10g01590 | A10 | 769816 | C | T | upstream_gene_variant | MODIFIER | c.-3591C>T| |
S270 |
4 | BAA10g01590 | A10 | 770273 | C | T | upstream_gene_variant | MODIFIER | c.-3134C>T| |
S113 |
5 | BAA10g01590 | A10 | 770939 | G | A | upstream_gene_variant | MODIFIER | c.-2468G>A| |
S121 |
6 | BAA10g01590 | A10 | 773479 | C | T | missense_variant | MODERATE | c.73C>T|p.Arg25Cys |
S249 |
7 | BAA10g01590 | A10 | 775877 | C | T | missense_variant | MODERATE | c.550C>T|p.Leu184Phe |
S34 |
8 | BAA10g01590 | A10 | 776521 | G | A | missense_variant | MODERATE | c.947G>A|p.Ser316Asn |
S192 |
9 | BAA10g01590 | A10 | 776551 | G | A | missense_variant | MODERATE | c.977G>A|p.Ser326Asn |
S158 |
10 | BAA10g01590 | A10 | 780702 | C | T | downstream_gene_variant | MODIFIER | c.*3054C>T| |
S235 |
11 | BAA10g01590 | A10 | 781402 | C | T | downstream_gene_variant | MODIFIER | c.*3754C>T| |
S110 |