Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g60620 | A09 | 58106100 | G | A | downstream_gene_variant | MODIFIER | c.*999C>T| |
S230 |
2 | BAA09g60620 | A09 | 58106805 | G | A | downstream_gene_variant | MODIFIER | c.*294C>T| |
S98 |
3 | BAA09g60620 | A09 | 58106828 | C | T | downstream_gene_variant | MODIFIER | c.*271G>A| |
S221 |
4 | BAA09g60620 | A09 | 58107058 | C | T | downstream_gene_variant | MODIFIER | c.*41G>A| |
S9 |
5 | BAA09g60620 | A09 | 58107857 | G | A | intron_variant | MODIFIER | c.446-68C>T| |
S65 |
6 | BAA09g60620 | A09 | 58108394 | C | T | intron_variant | MODIFIER | c.207-37G>A| |
S114 |
7 | BAA09g60620 | A09 | 58108785 | C | T | intron_variant | MODIFIER | c.207-428G>A| |
S108 |
8 | BAA09g60620 | A09 | 58109176 | G | A | intron_variant | MODIFIER | c.207-819C>T| |
S160 |
9 | BAA09g60620 | A09 | 58109993 | C | T | intron_variant | MODIFIER | c.206+28G>A| |
S272 |
10 | BAA09g60620 | A09 | 58110058 | C | T | missense_variant | MODERATE | c.169G>A|p.Asp57Asn |
S281 |
11 | BAA09g60620 | A09 | 58110360 | C | T | upstream_gene_variant | MODIFIER | c.-134G>A| |
S206 |
12 | BAA09g60620 | A09 | 58110696 | G | A | upstream_gene_variant | MODIFIER | c.-470C>T| |
S257 |