Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g00970 | A06 | 656768 | C | T | upstream_gene_variant | MODIFIER | c.-4783C>T| |
S158 |
2 | BAA06g00970 | A06 | 658467 | G | A | upstream_gene_variant | MODIFIER | c.-3084G>A| |
S191 |
3 | BAA06g00970 | A06 | 658932 | G | A | upstream_gene_variant | MODIFIER | c.-2619G>A| |
S125 |
4 | BAA06g00970 | A06 | 659092 | C | T | upstream_gene_variant | MODIFIER | c.-2459C>T| |
S18 |
5 | BAA06g00970 | A06 | 660567 | C | T | upstream_gene_variant | MODIFIER | c.-984C>T| |
S184 |
6 | BAA06g00970 | A06 | 660862 | G | A | upstream_gene_variant | MODIFIER | c.-689G>A| |
S144 |
7 | BAA06g00970 | A06 | 661315 | C | T | upstream_gene_variant | MODIFIER | c.-236C>T| |
S34 |
8 | BAA06g00970 | A06 | 662077 | C | T | missense_variant | MODERATE | c.527C>T|p.Ser176Phe |
S136 |
9 | BAA06g00970 | A06 | 663337 | G | A | downstream_gene_variant | MODIFIER | c.*1004G>A| |
S155 |
10 | BAA06g00970 | A06 | 664167 | C | T | downstream_gene_variant | MODIFIER | c.*1834C>T| |
S221 |
11 | BAA06g00970 | A06 | 664169 | C | T | downstream_gene_variant | MODIFIER | c.*1836C>T| |
S133 |
12 | BAA06g00970 | A06 | 664480 | G | A | downstream_gene_variant | MODIFIER | c.*2147G>A| |
S191 |
13 | BAA06g00970 | A06 | 664988 | C | T | downstream_gene_variant | MODIFIER | c.*2655C>T| |
S219 S72 |
14 | BAA06g00970 | A06 | 666592 | G | A | downstream_gene_variant | MODIFIER | c.*4259G>A| |
S69 |
15 | BAA06g00970 | A06 | 666594 | G | A | downstream_gene_variant | MODIFIER | c.*4261G>A| |
S53 |
16 | BAA06g00970 | A06 | 666619 | C | T | downstream_gene_variant | MODIFIER | c.*4286C>T| |
S228 |
17 | BAA06g00970 | A06 | 666947 | G | A | downstream_gene_variant | MODIFIER | c.*4614G>A| |
S159 S299 |