Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05660 | A10 | 2897542 | G | A | missense_variant | MODERATE | c.2408C>T|p.Thr803Ile |
S138 |
2 | BAA10g05660 | A10 | 2899741 | C | T | synonymous_variant | LOW | c.1200G>A|p.Gln400Gln |
S119 |
3 | BAA10g05660 | A10 | 2901075 | C | T | intron_variant | MODIFIER | c.755+62G>A| |
S205 |
4 | BAA10g05660 | A10 | 2902163 | C | T | intron_variant | MODIFIER | c.248+59G>A| |
S2 |
5 | BAA10g05660 | A10 | 2903853 | G | A | upstream_gene_variant | MODIFIER | c.-1283C>T| |
S296 |
6 | BAA10g05660 | A10 | 2904250 | G | A | upstream_gene_variant | MODIFIER | c.-1680C>T| |
S179 |
7 | BAA10g05660 | A10 | 2904713 | G | A | upstream_gene_variant | MODIFIER | c.-2143C>T| |
S230 |
8 | BAA10g05660 | A10 | 2904807 | C | T | upstream_gene_variant | MODIFIER | c.-2237G>A| |
S143 |
9 | BAA10g05660 | A10 | 2905350 | C | T | upstream_gene_variant | MODIFIER | c.-2780G>A| |
S68 |
10 | BAA10g05660 | A10 | 2905589 | G | A | upstream_gene_variant | MODIFIER | c.-3019C>T| |
S48 |
11 | BAA10g05660 | A10 | 2905701 | C | T | upstream_gene_variant | MODIFIER | c.-3131G>A| |
S269 |
12 | BAA10g05660 | A10 | 2905868 | C | T | upstream_gene_variant | MODIFIER | c.-3298G>A| |
S177 |
13 | BAA10g05660 | A10 | 2905919 | G | A | upstream_gene_variant | MODIFIER | c.-3349C>T| |
S182 |
14 | BAA10g05660 | A10 | 2906283 | G | A | upstream_gene_variant | MODIFIER | c.-3713C>T| |
S68 |
15 | BAA10g05660 | A10 | 2906428 | C | T | upstream_gene_variant | MODIFIER | c.-3858G>A| |
S114 S25 |
16 | BAA10g05660 | A10 | 2906591 | C | T | upstream_gene_variant | MODIFIER | c.-4021G>A| |
S42 |
17 | BAA10g05660 | A10 | 2907459 | A | G | upstream_gene_variant | MODIFIER | c.-4889T>C| |
S215 |