Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g10440 | A09 | 5711592 | G | A | upstream_gene_variant | MODIFIER | c.-2285G>A| |
S146 |
2 | BAA09g10440 | A09 | 5712093 | C | T | upstream_gene_variant | MODIFIER | c.-1784C>T| |
S263 |
3 | BAA09g10440 | A09 | 5712751 | G | A | upstream_gene_variant | MODIFIER | c.-1126G>A| |
S61 |
4 | BAA09g10440 | A09 | 5712858 | C | T | upstream_gene_variant | MODIFIER | c.-1019C>T| |
S9 |
5 | BAA09g10440 | A09 | 5712992 | G | A | upstream_gene_variant | MODIFIER | c.-885G>A| |
S302 |
6 | BAA09g10440 | A09 | 5713082 | G | A | upstream_gene_variant | MODIFIER | c.-795G>A| |
S12 |
7 | BAA09g10440 | A09 | 5713423 | C | T | upstream_gene_variant | MODIFIER | c.-454C>T| |
S270 |
8 | BAA09g10440 | A09 | 5713721 | G | A | upstream_gene_variant | MODIFIER | c.-156G>A| |
S69 |
9 | BAA09g10440 | A09 | 5715441 | C | T | missense_variant | MODERATE | c.950C>T|p.Ser317Phe |
S202 |
10 | BAA09g10440 | A09 | 5717792 | G | A | missense_variant | MODERATE | c.2110G>A|p.Val704Ile |
S73 S91 |
11 | BAA09g10440 | A09 | 5718009 | C | T | missense_variant | MODERATE | c.2240C>T|p.Thr747Ile |
S132 S137 S215 |
12 | BAA09g10440 | A09 | 5718694 | G | A | synonymous_variant | LOW | c.2661G>A|p.Glu887Glu |
S149 |
13 | BAA09g10440 | A09 | 5718697 | G | A | synonymous_variant | LOW | c.2664G>A|p.Lys888Lys |
S4 |
14 | BAA09g10440 | A09 | 5719485 | C | T | missense_variant | MODERATE | c.2959C>T|p.Leu987Phe |
S302 |