Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g20000 | A10 | 18164650 | C | T | upstream_gene_variant | MODIFIER | c.-3894C>T| |
S199 |
2 | BAA10g20000 | A10 | 18165324 | C | T | upstream_gene_variant | MODIFIER | c.-3220C>T| |
S305 |
3 | BAA10g20000 | A10 | 18165386 | C | T | upstream_gene_variant | MODIFIER | c.-3158C>T| |
S99 |
4 | BAA10g20000 | A10 | 18165670 | G | A | upstream_gene_variant | MODIFIER | c.-2874G>A| |
S239 |
5 | BAA10g20000 | A10 | 18166436 | G | A | upstream_gene_variant | MODIFIER | c.-2108G>A| |
S284 |
6 | BAA10g20000 | A10 | 18166717 | C | T | upstream_gene_variant | MODIFIER | c.-1827C>T| |
S99 |
7 | BAA10g20000 | A10 | 18167636 | A | G | upstream_gene_variant | MODIFIER | c.-908A>G| |
S147 S151 S199 S229 |
8 | BAA10g20000 | A10 | 18168993 | G | A | missense_variant | MODERATE | c.152G>A|p.Ser51Asn |
S67 |
9 | BAA10g20000 | A10 | 18170341 | G | A | missense_variant | MODERATE | c.919G>A|p.Gly307Arg |
S223 |
10 | BAA10g20000 | A10 | 18171305 | C | T | stop_gained | HIGH | c.1705C>T|p.Gln569* |
S204 |
11 | BAA10g20000 | A10 | 18171737 | C | T | synonymous_variant | LOW | c.2137C>T|p.Leu713Leu |
S44 |
12 | BAA10g20000 | A10 | 18173465 | C | T | downstream_gene_variant | MODIFIER | c.*111C>T| |
S268 |
13 | BAA10g20000 | A10 | 18173498 | C | T | downstream_gene_variant | MODIFIER | c.*144C>T| |
S87 |
14 | BAA10g20000 | A10 | 18174069 | G | A | downstream_gene_variant | MODIFIER | c.*715G>A| |
S291 |