Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g17580 | A06 | 8915890 | G | A | downstream_gene_variant | MODIFIER | c.*3946C>T| |
S105 S106 |
2 | BAA06g17580 | A06 | 8915992 | G | A | downstream_gene_variant | MODIFIER | c.*3844C>T| |
S256 |
3 | BAA06g17580 | A06 | 8916658 | G | A | downstream_gene_variant | MODIFIER | c.*3178C>T| |
S144 |
4 | BAA06g17580 | A06 | 8916747 | G | A | downstream_gene_variant | MODIFIER | c.*3089C>T| |
S140 |
5 | BAA06g17580 | A06 | 8916765 | G | A | downstream_gene_variant | MODIFIER | c.*3071C>T| |
S261 |
6 | BAA06g17580 | A06 | 8919070 | G | A | downstream_gene_variant | MODIFIER | c.*766C>T| |
S262 |
7 | BAA06g17580 | A06 | 8919389 | C | T | downstream_gene_variant | MODIFIER | c.*447G>A| |
S62 |
8 | BAA06g17580 | A06 | 8919488 | G | A | downstream_gene_variant | MODIFIER | c.*348C>T| |
S1 |
9 | BAA06g17580 | A06 | 8920074 | C | T | missense_variant | MODERATE | c.1622G>A|p.Gly541Glu |
S301 |
10 | BAA06g17580 | A06 | 8920855 | G | A | missense_variant | MODERATE | c.1214C>T|p.Thr405Ile |
S292 |
11 | BAA06g17580 | A06 | 8923555 | G | A | missense_variant | MODERATE | c.68C>T|p.Pro23Leu |
S82 S92 |
12 | BAA06g17580 | A06 | 8923771 | G | A | upstream_gene_variant | MODIFIER | c.-149C>T| |
S182 |
13 | BAA06g17580 | A06 | 8924036 | G | A | upstream_gene_variant | MODIFIER | c.-414C>T| |
S15 S3 |
14 | BAA06g17580 | A06 | 8924050 | C | T | upstream_gene_variant | MODIFIER | c.-428G>A| |
S178 S186 |
15 | BAA06g17580 | A06 | 8924578 | C | T | upstream_gene_variant | MODIFIER | c.-956G>A| |
S164 |
16 | BAA06g17580 | A06 | 8927960 | C | T | upstream_gene_variant | MODIFIER | c.-4338G>A| |
S163 |
17 | BAA06g17580 | A06 | 8928557 | G | A | upstream_gene_variant | MODIFIER | c.-4935C>T| |
S144 |