Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g41000 | A06 | 26729207 | G | A | upstream_gene_variant | MODIFIER | c.-4866G>A| |
S302 |
2 | BAA06g41000 | A06 | 26729619 | C | T | upstream_gene_variant | MODIFIER | c.-4454C>T| |
S242 |
3 | BAA06g41000 | A06 | 26729916 | C | T | upstream_gene_variant | MODIFIER | c.-4157C>T| |
S252 |
4 | BAA06g41000 | A06 | 26729969 | G | A | upstream_gene_variant | MODIFIER | c.-4104G>A| |
S160 |
5 | BAA06g41000 | A06 | 26730736 | C | T | upstream_gene_variant | MODIFIER | c.-3337C>T| |
S153 |
6 | BAA06g41000 | A06 | 26732008 | C | T | upstream_gene_variant | MODIFIER | c.-2065C>T| |
S180 |
7 | BAA06g41000 | A06 | 26733414 | C | T | upstream_gene_variant | MODIFIER | c.-659C>T| |
S112 |
8 | BAA06g41000 | A06 | 26733432 | G | A | upstream_gene_variant | MODIFIER | c.-641G>A| |
S233 |
9 | BAA06g41000 | A06 | 26734583 | C | T | missense_variant | MODERATE | c.511C>T|p.His171Tyr |
S52 |
10 | BAA06g41000 | A06 | 26736666 | C | T | missense_variant | MODERATE | c.1381C>T|p.Leu461Phe |
S182 |