Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g05630 | A08 | 4317587 | G | A | missense_variant | MODERATE | c.403G>A|p.Val135Ile |
S187 |
2 | BAA08g05630 | A08 | 4317770 | G | A | synonymous_variant | LOW | c.507G>A|p.Gln169Gln |
S98 |
3 | BAA08g05630 | A08 | 4318821 | G | A | missense_variant | MODERATE | c.1154G>A|p.Gly385Asp |
S281 |
4 | BAA08g05630 | A08 | 4319243 | G | A | missense_variant | MODERATE | c.1408G>A|p.Val470Ile |
S72 S78 |
5 | BAA08g05630 | A08 | 4319798 | C | T | missense_variant | MODERATE | c.1604C>T|p.Ser535Phe |
S172 S217 |
6 | BAA08g05630 | A08 | 4320691 | G | A | missense_variant | MODERATE | c.1849G>A|p.Gly617Arg |
S297 |
7 | BAA08g05630 | A08 | 4324723 | C | T | downstream_gene_variant | MODIFIER | c.*3523C>T| |
S66 |
8 | BAA08g05630 | A08 | 4324852 | C | T | downstream_gene_variant | MODIFIER | c.*3652C>T| |
S138 |
9 | BAA08g05630 | A08 | 4325043 | G | A | downstream_gene_variant | MODIFIER | c.*3843G>A| |
S154 |
10 | BAA08g05630 | A08 | 4325118 | G | A | downstream_gene_variant | MODIFIER | c.*3918G>A| |
S129 |
11 | BAA08g05630 | A08 | 4326132 | C | T | downstream_gene_variant | MODIFIER | c.*4932C>T| |
S4 |