Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g07900 | A10 | 4992510 | C | T | upstream_gene_variant | MODIFIER | c.-4757C>T| |
S42 |
2 | BAA10g07900 | A10 | 4995515 | G | A | upstream_gene_variant | MODIFIER | c.-1752G>A| |
S125 |
3 | BAA10g07900 | A10 | 4996860 | C | T | upstream_gene_variant | MODIFIER | c.-407C>T| |
S193 |
4 | BAA10g07900 | A10 | 4996945 | G | A | upstream_gene_variant | MODIFIER | c.-322G>A| |
S237 |
5 | BAA10g07900 | A10 | 4997379 | G | A | missense_variant | MODERATE | c.113G>A|p.Arg38Lys |
S62 |
6 | BAA10g07900 | A10 | 4997520 | G | A | intron_variant | MODIFIER | c.175-38G>A| |
S283 |
7 | BAA10g07900 | A10 | 4997763 | G | A | missense_variant | MODERATE | c.380G>A|p.Arg127Lys |
S219 S72 |
8 | BAA10g07900 | A10 | 4999430 | C | T | downstream_gene_variant | MODIFIER | c.*1099C>T| |
S87 |
9 | BAA10g07900 | A10 | 4999608 | C | T | downstream_gene_variant | MODIFIER | c.*1277C>T| |
S98 |
10 | BAA10g07900 | A10 | 4999970 | G | A | downstream_gene_variant | MODIFIER | c.*1639G>A| |
S292 |
11 | BAA10g07900 | A10 | 5001218 | C | T | downstream_gene_variant | MODIFIER | c.*2887C>T| |
S196 |
12 | BAA10g07900 | A10 | 5001410 | C | T | downstream_gene_variant | MODIFIER | c.*3079C>T| |
S47 |
13 | BAA10g07900 | A10 | 5001527 | C | T | downstream_gene_variant | MODIFIER | c.*3196C>T| |
S74 |
14 | BAA10g07900 | A10 | 5002524 | C | T | downstream_gene_variant | MODIFIER | c.*4193C>T| |
S114 |
15 | BAA10g07900 | A10 | 5002687 | C | T | downstream_gene_variant | MODIFIER | c.*4356C>T| |
S242 |
16 | BAA10g07900 | A10 | 5002714 | C | T | downstream_gene_variant | MODIFIER | c.*4383C>T| |
S159 S243 S299 |