Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17280 | A10 | 16710140 | G | A | downstream_gene_variant | MODIFIER | c.*2658C>T| |
S194 |
2 | BAA10g17280 | A10 | 16710448 | C | T | downstream_gene_variant | MODIFIER | c.*2350G>A| |
S46 |
3 | BAA10g17280 | A10 | 16710622 | G | A | downstream_gene_variant | MODIFIER | c.*2176C>T| |
S271 |
4 | BAA10g17280 | A10 | 16710743 | G | A | downstream_gene_variant | MODIFIER | c.*2055C>T| |
S240 |
5 | BAA10g17280 | A10 | 16710794 | C | T | downstream_gene_variant | MODIFIER | c.*2004G>A| |
S170 |
6 | BAA10g17280 | A10 | 16710852 | G | A | downstream_gene_variant | MODIFIER | c.*1946C>T| |
S59 |
7 | BAA10g17280 | A10 | 16711906 | C | T | downstream_gene_variant | MODIFIER | c.*892G>A| |
S48 |
8 | BAA10g17280 | A10 | 16712019 | C | T | downstream_gene_variant | MODIFIER | c.*779G>A| |
S201 |
9 | BAA10g17280 | A10 | 16712616 | G | A | downstream_gene_variant | MODIFIER | c.*182C>T| |
S1 S90 |
10 | BAA10g17280 | A10 | 16712852 | C | T | missense_variant | MODERATE | c.1140G>A|p.Met380Ile |
S190 |
11 | BAA10g17280 | A10 | 16713577 | C | T | missense_variant | MODERATE | c.415G>A|p.Glu139Lys |
S246 |
12 | BAA10g17280 | A10 | 16717574 | G | A | upstream_gene_variant | MODIFIER | c.-3583C>T| |
S276 |
13 | BAA10g17280 | A10 | 16718635 | G | A | upstream_gene_variant | MODIFIER | c.-4644C>T| |
S17 |
14 | BAA10g17280 | A10 | 16718637 | G | A | upstream_gene_variant | MODIFIER | c.-4646C>T| |
S126 |
15 | BAA10g17280 | A10 | 16718667 | C | T | upstream_gene_variant | MODIFIER | c.-4676G>A| |
S47 |