Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05650 | A08 | 4332335 | C | T | downstream_gene_variant | MODIFIER | c.*4700G>A| |
S205 |
2 | BAA08g05650 | A08 | 4333322 | C | T | downstream_gene_variant | MODIFIER | c.*3713G>A| |
S28 |
3 | BAA08g05650 | A08 | 4333916 | G | A | downstream_gene_variant | MODIFIER | c.*3119C>T| |
S37 |
4 | BAA08g05650 | A08 | 4335843 | C | T | downstream_gene_variant | MODIFIER | c.*1192G>A| |
S162 |
5 | BAA08g05650 | A08 | 4336365 | G | A | downstream_gene_variant | MODIFIER | c.*670C>T| |
S43 |
6 | BAA08g05650 | A08 | 4336842 | G | A | downstream_gene_variant | MODIFIER | c.*193C>T| |
S298 |
7 | BAA08g05650 | A08 | 4336989 | C | T | downstream_gene_variant | MODIFIER | c.*46G>A| |
S175 |
8 | BAA08g05650 | A08 | 4337441 | G | A | intron_variant | MODIFIER | c.1044+28C>T| |
S148 |
9 | BAA08g05650 | A08 | 4337621 | G | A | missense_variant | MODERATE | c.892C>T|p.Leu298Phe |
S179 |
10 | BAA08g05650 | A08 | 4338309 | G | A | missense_variant | MODERATE | c.446C>T|p.Ser149Phe |
S11 |
11 | BAA08g05650 | A08 | 4338958 | G | T | upstream_gene_variant | MODIFIER | c.-71C>A| |
S68 |
12 | BAA08g05650 | A08 | 4339019 | G | A | upstream_gene_variant | MODIFIER | c.-132C>T| |
S188 |
13 | BAA08g05650 | A08 | 4339280 | G | A | upstream_gene_variant | MODIFIER | c.-393C>T| |
S130 |
14 | BAA08g05650 | A08 | 4339652 | G | A | upstream_gene_variant | MODIFIER | c.-765C>T| |
S68 |
15 | BAA08g05650 | A08 | 4341249 | C | T | upstream_gene_variant | MODIFIER | c.-2362G>A| |
S192 |
16 | BAA08g05650 | A08 | 4342522 | G | A | upstream_gene_variant | MODIFIER | c.-3635C>T| |
S128 |