Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g17380 | A09 | 10378480 | C | T | upstream_gene_variant | MODIFIER | c.-4324C>T| |
S109 |
2 | BAA09g17380 | A09 | 10379308 | C | T | upstream_gene_variant | MODIFIER | c.-3496C>T| |
S6 |
3 | BAA09g17380 | A09 | 10380479 | G | A | upstream_gene_variant | MODIFIER | c.-2325G>A| |
S191 |
4 | BAA09g17380 | A09 | 10380945 | C | T | upstream_gene_variant | MODIFIER | c.-1859C>T| |
S92 |
5 | BAA09g17380 | A09 | 10381282 | G | A | upstream_gene_variant | MODIFIER | c.-1522G>A| |
S207 |
6 | BAA09g17380 | A09 | 10381835 | G | A | upstream_gene_variant | MODIFIER | c.-969G>A| |
S45 |
7 | BAA09g17380 | A09 | 10382074 | C | T | upstream_gene_variant | MODIFIER | c.-730C>T| |
S146 |
8 | BAA09g17380 | A09 | 10383266 | G | A | missense_variant | MODERATE | c.463G>A|p.Asp155Asn |
S46 |
9 | BAA09g17380 | A09 | 10383400 | G | A | missense_variant | MODERATE | c.597G>A|p.Met199Ile |
S149 |
10 | BAA09g17380 | A09 | 10389112 | C | T | downstream_gene_variant | MODIFIER | c.*4925C>T| |
S71 |