Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g42730 | A09 | 49011529 | C | T | upstream_gene_variant | MODIFIER | c.-4854C>T| |
S43 |
2 | BAA09g42730 | A09 | 49011726 | C | T | upstream_gene_variant | MODIFIER | c.-4657C>T| |
S5 |
3 | BAA09g42730 | A09 | 49011765 | C | T | upstream_gene_variant | MODIFIER | c.-4618C>T| |
S181 S250 |
4 | BAA09g42730 | A09 | 49013464 | C | T | upstream_gene_variant | MODIFIER | c.-2919C>T| |
S302 |
5 | BAA09g42730 | A09 | 49014494 | G | A | upstream_gene_variant | MODIFIER | c.-1889G>A| |
S271 |
6 | BAA09g42730 | A09 | 49014659 | G | A | upstream_gene_variant | MODIFIER | c.-1724G>A| |
S249 |
7 | BAA09g42730 | A09 | 49015198 | G | A | upstream_gene_variant | MODIFIER | c.-1185G>A| |
S239 |
8 | BAA09g42730 | A09 | 49016465 | C | T | missense_variant | MODERATE | c.83C>T|p.Ser28Phe |
S276 |
9 | BAA09g42730 | A09 | 49016581 | C | T | intron_variant | MODIFIER | c.184+15C>T| |
S223 |
10 | BAA09g42730 | A09 | 49016891 | G | A | missense_variant | MODERATE | c.409G>A|p.Glu137Lys |
S210 S225 |
11 | BAA09g42730 | A09 | 49017548 | G | A | downstream_gene_variant | MODIFIER | c.*328G>A| |
S86 |
12 | BAA09g42730 | A09 | 49019031 | G | A | downstream_gene_variant | MODIFIER | c.*1811G>A| |
S34 |
13 | BAA09g42730 | A09 | 49019957 | G | A | downstream_gene_variant | MODIFIER | c.*2737G>A| |
S42 |
14 | BAA09g42730 | A09 | 49021228 | G | A | downstream_gene_variant | MODIFIER | c.*4008G>A| |
S161 |
15 | BAA09g42730 | A09 | 49021706 | G | A | downstream_gene_variant | MODIFIER | c.*4486G>A| |
S74 |