Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g14470 | A10 | 15162340 | C | T | upstream_gene_variant | MODIFIER | c.-4998C>T| |
S170 |
2 | BAA10g14470 | A10 | 15162575 | C | T | upstream_gene_variant | MODIFIER | c.-4763C>T| |
S143 |
3 | BAA10g14470 | A10 | 15162762 | C | T | upstream_gene_variant | MODIFIER | c.-4576C>T| |
S244 |
4 | BAA10g14470 | A10 | 15163287 | C | T | upstream_gene_variant | MODIFIER | c.-4051C>T| |
S202 |
5 | BAA10g14470 | A10 | 15163627 | T | C | upstream_gene_variant | MODIFIER | c.-3711T>C| |
S107 |
6 | BAA10g14470 | A10 | 15163689 | C | T | upstream_gene_variant | MODIFIER | c.-3649C>T| |
S6 |
7 | BAA10g14470 | A10 | 15164138 | C | T | upstream_gene_variant | MODIFIER | c.-3200C>T| |
S133 |
8 | BAA10g14470 | A10 | 15164563 | C | T | upstream_gene_variant | MODIFIER | c.-2775C>T| |
S173 |
9 | BAA10g14470 | A10 | 15165546 | C | T | upstream_gene_variant | MODIFIER | c.-1792C>T| |
S96 |
10 | BAA10g14470 | A10 | 15167351 | G | A | missense_variant | MODERATE | c.14G>A|p.Gly5Glu |
S181 |
11 | BAA10g14470 | A10 | 15167622 | G | A | missense_variant | MODERATE | c.170G>A|p.Gly57Glu |
S94 |
12 | BAA10g14470 | A10 | 15168274 | G | A | synonymous_variant | LOW | c.822G>A|p.Glu274Glu |
S64 |