Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g13700 | A10 | 14643564 | G | A | upstream_gene_variant | MODIFIER | c.-4782G>A| |
S68 |
2 | BAA10g13700 | A10 | 14644232 | C | T | upstream_gene_variant | MODIFIER | c.-4114C>T| |
S175 |
3 | BAA10g13700 | A10 | 14644645 | A | T | upstream_gene_variant | MODIFIER | c.-3701A>T| |
S215 |
4 | BAA10g13700 | A10 | 14644704 | G | A | upstream_gene_variant | MODIFIER | c.-3642G>A| |
S59 |
5 | BAA10g13700 | A10 | 14645661 | G | A | upstream_gene_variant | MODIFIER | c.-2685G>A| |
S164 |
6 | BAA10g13700 | A10 | 14646684 | G | A | upstream_gene_variant | MODIFIER | c.-1662G>A| |
S192 S245 |
7 | BAA10g13700 | A10 | 14647218 | G | A | upstream_gene_variant | MODIFIER | c.-1128G>A| |
S239 |
8 | BAA10g13700 | A10 | 14648691 | C | T | missense_variant | MODERATE | c.346C>T|p.Pro116Ser |
S229 |
9 | BAA10g13700 | A10 | 14651267 | C | T | downstream_gene_variant | MODIFIER | c.*1660C>T| |
S63 |
10 | BAA10g13700 | A10 | 14651420 | C | T | downstream_gene_variant | MODIFIER | c.*1813C>T| |
S5 |
11 | BAA10g13700 | A10 | 14653319 | G | A | downstream_gene_variant | MODIFIER | c.*3712G>A| |
S292 |
12 | BAA10g13700 | A10 | 14654031 | G | A | downstream_gene_variant | MODIFIER | c.*4424G>A| |
S61 |