Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00170 | A08 | 129279 | C | T | upstream_gene_variant | MODIFIER | c.-4526C>T| |
S6 |
2 | BAA08g00170 | A08 | 129389 | C | T | upstream_gene_variant | MODIFIER | c.-4416C>T| |
S43 |
3 | BAA08g00170 | A08 | 130563 | A | C | upstream_gene_variant | MODIFIER | c.-3242A>C| |
S303 |
4 | BAA08g00170 | A08 | 130773 | C | T | upstream_gene_variant | MODIFIER | c.-3032C>T| |
S136 |
5 | BAA08g00170 | A08 | 130859 | C | T | upstream_gene_variant | MODIFIER | c.-2946C>T| |
S189 |
6 | BAA08g00170 | A08 | 131966 | C | T | upstream_gene_variant | MODIFIER | c.-1839C>T| |
S216 |
7 | BAA08g00170 | A08 | 133902 | C | T | missense_variant | MODERATE | c.98C>T|p.Ser33Phe |
S163 |
8 | BAA08g00170 | A08 | 134902 | C | T | downstream_gene_variant | MODIFIER | c.*801C>T| |
S59 |
9 | BAA08g00170 | A08 | 135064 | C | T | downstream_gene_variant | MODIFIER | c.*963C>T| |
S18 |
10 | BAA08g00170 | A08 | 135182 | G | A | downstream_gene_variant | MODIFIER | c.*1081G>A| |
S262 |
11 | BAA08g00170 | A08 | 137322 | C | T | downstream_gene_variant | MODIFIER | c.*3221C>T| |
S275 |