Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g53930 | A09 | 54872981 | G | A | upstream_gene_variant | MODIFIER | c.-3966G>A| |
S216 |
2 | BAA09g53930 | A09 | 54873522 | C | T | upstream_gene_variant | MODIFIER | c.-3425C>T| |
S41 |
3 | BAA09g53930 | A09 | 54874809 | T | A | upstream_gene_variant | MODIFIER | c.-2138T>A| |
S306 |
4 | BAA09g53930 | A09 | 54876315 | G | A | upstream_gene_variant | MODIFIER | c.-632G>A| |
S255 |
5 | BAA09g53930 | A09 | 54877015 | G | A | synonymous_variant | LOW | c.69G>A|p.Arg23Arg |
S58 |
6 | BAA09g53930 | A09 | 54877444 | C | T | intron_variant | MODIFIER | c.176+322C>T| |
S156 |
7 | BAA09g53930 | A09 | 54878634 | G | A | intron_variant | MODIFIER | c.177-973G>A| |
S172 S217 |
8 | BAA09g53930 | A09 | 54878777 | G | A | intron_variant | MODIFIER | c.177-830G>A| |
S268 |
9 | BAA09g53930 | A09 | 54878852 | C | T | intron_variant | MODIFIER | c.177-755C>T| |
S230 |
10 | BAA09g53930 | A09 | 54880692 | C | T | intron_variant | MODIFIER | c.549+713C>T| |
S9 |
11 | BAA09g53930 | A09 | 54881291 | C | T | intron_variant | MODIFIER | c.550-1094C>T| |
S117 |
12 | BAA09g53930 | A09 | 54881668 | C | T | intron_variant | MODIFIER | c.550-717C>T| |
S203 |
13 | BAA09g53930 | A09 | 54881829 | G | A | intron_variant | MODIFIER | c.550-556G>A| |
S193 |
14 | BAA09g53930 | A09 | 54883429 | C | T | missense_variant | MODERATE | c.1322C>T|p.Ala441Val |
S245 |
15 | BAA09g53930 | A09 | 54883480 | C | T | missense_variant | MODERATE | c.1373C>T|p.Ser458Phe |
S302 |
16 | BAA09g53930 | A09 | 54889034 | G | A | downstream_gene_variant | MODIFIER | c.*4686G>A| |
S12 |