Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g20790 | A06 | 11095071 | G | A | upstream_gene_variant | MODIFIER | c.-4016G>A| |
S53 |
2 | BAA06g20790 | A06 | 11096751 | G | A | upstream_gene_variant | MODIFIER | c.-2336G>A| |
S20 |
3 | BAA06g20790 | A06 | 11096867 | C | T | upstream_gene_variant | MODIFIER | c.-2220C>T| |
S116 |
4 | BAA06g20790 | A06 | 11096939 | C | T | upstream_gene_variant | MODIFIER | c.-2148C>T| |
S298 |
5 | BAA06g20790 | A06 | 11097761 | G | A | upstream_gene_variant | MODIFIER | c.-1326G>A| |
S146 |
6 | BAA06g20790 | A06 | 11097887 | G | A | upstream_gene_variant | MODIFIER | c.-1200G>A| |
S308 |
7 | BAA06g20790 | A06 | 11098279 | G | A | upstream_gene_variant | MODIFIER | c.-808G>A| |
S186 S216 |
8 | BAA06g20790 | A06 | 11098455 | G | A | upstream_gene_variant | MODIFIER | c.-632G>A| |
S7 |
9 | BAA06g20790 | A06 | 11098721 | G | A | upstream_gene_variant | MODIFIER | c.-366G>A| |
S130 |
10 | BAA06g20790 | A06 | 11100464 | G | A | missense_variant | MODERATE | c.601G>A|p.Asp201Asn |
S210 S225 |
11 | BAA06g20790 | A06 | 11104628 | G | A | downstream_gene_variant | MODIFIER | c.*3967G>A| |
S69 |
12 | BAA06g20790 | A06 | 11105166 | G | A | downstream_gene_variant | MODIFIER | c.*4505G>A| |
S221 |