Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g00230 | A08 | 186497 | C | T | missense_variant | MODERATE | c.679G>A|p.Asp227Asn |
S148 S210 S30 S31 |
2 | BAA08g00230 | A08 | 187053 | G | A | missense_variant | MODERATE | c.206C>T|p.Pro69Leu |
S107 |
3 | BAA08g00230 | A08 | 187492 | G | A | upstream_gene_variant | MODIFIER | c.-234C>T| |
S211 |
4 | BAA08g00230 | A08 | 187594 | C | G | upstream_gene_variant | MODIFIER | c.-336G>C| |
S302 |
5 | BAA08g00230 | A08 | 189385 | G | A | upstream_gene_variant | MODIFIER | c.-2127C>T| |
S262 |
6 | BAA08g00230 | A08 | 190514 | C | T | upstream_gene_variant | MODIFIER | c.-3256G>A| |
S163 |
7 | BAA08g00230 | A08 | 190673 | G | A | upstream_gene_variant | MODIFIER | c.-3415C>T| |
S16 |
8 | BAA08g00230 | A08 | 192110 | C | T | upstream_gene_variant | MODIFIER | c.-4852G>A| |
S56 |
9 | BAA08g00230 | A08 | 192189 | C | T | upstream_gene_variant | MODIFIER | c.-4931G>A| |
S173 |