Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g24890 | A08 | 18095016 | G | A | upstream_gene_variant | MODIFIER | c.-3052G>A| |
S221 |
2 | BAA08g24890 | A08 | 18095590 | C | T | upstream_gene_variant | MODIFIER | c.-2478C>T| |
S81 S85 |
3 | BAA08g24890 | A08 | 18096006 | G | A | upstream_gene_variant | MODIFIER | c.-2062G>A| |
S119 S130 S159 S161 S166 S183 S299 S305 S47 S53 |
4 | BAA08g24890 | A08 | 18096081 | C | T | upstream_gene_variant | MODIFIER | c.-1987C>T| |
S104 S52 |
5 | BAA08g24890 | A08 | 18096281 | G | A | upstream_gene_variant | MODIFIER | c.-1787G>A| |
S109 |
6 | BAA08g24890 | A08 | 18096540 | C | T | upstream_gene_variant | MODIFIER | c.-1528C>T| |
S189 |
7 | BAA08g24890 | A08 | 18097021 | C | T | upstream_gene_variant | MODIFIER | c.-1047C>T| |
S210 |
8 | BAA08g24890 | A08 | 18098218 | C | T | missense_variant | MODERATE | c.151C>T|p.Leu51Phe |
S224 |
9 | BAA08g24890 | A08 | 18098405 | C | T | missense_variant | MODERATE | c.338C>T|p.Thr113Ile |
S69 |
10 | BAA08g24890 | A08 | 18100557 | G | A | downstream_gene_variant | MODIFIER | c.*1755G>A| |
S241 |
11 | BAA08g24890 | A08 | 18101977 | G | A | downstream_gene_variant | MODIFIER | c.*3175G>A| |
S251 |
12 | BAA08g24890 | A08 | 18102908 | G | A | downstream_gene_variant | MODIFIER | c.*4106G>A| |
S122 |
13 | BAA08g24890 | A08 | 18103406 | G | A | downstream_gene_variant | MODIFIER | c.*4604G>A| |
S111 |