Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g11500 | A08 | 10192462 | C | T | upstream_gene_variant | MODIFIER | c.-1996C>T| |
S305 |
2 | BAA08g11500 | A08 | 10192612 | G | A | upstream_gene_variant | MODIFIER | c.-1846G>A| |
S5 |
3 | BAA08g11500 | A08 | 10192893 | C | T | upstream_gene_variant | MODIFIER | c.-1565C>T| |
S112 |
4 | BAA08g11500 | A08 | 10195536 | A | T | synonymous_variant | LOW | c.489A>T|p.Ala163Ala |
S150 |
5 | BAA08g11500 | A08 | 10195597 | C | T | splice_region_variant&intron_variant | LOW | c.547+3C>T| |
S302 |
6 | BAA08g11500 | A08 | 10195945 | G | A | missense_variant | MODERATE | c.638G>A|p.Gly213Glu |
S56 |
7 | BAA08g11500 | A08 | 10195968 | C | T | missense_variant | MODERATE | c.661C>T|p.Pro221Ser |
S236 |
8 | BAA08g11500 | A08 | 10195969 | C | T | missense_variant | MODERATE | c.662C>T|p.Pro221Leu |
S173 |
9 | BAA08g11500 | A08 | 10196343 | G | A | missense_variant | MODERATE | c.1036G>A|p.Asp346Asn |
S242 |
10 | BAA08g11500 | A08 | 10196928 | G | A | missense_variant | MODERATE | c.1441G>A|p.Gly481Ser |
S280 |
11 | BAA08g11500 | A08 | 10197143 | C | T | downstream_gene_variant | MODIFIER | c.*198C>T| |
S168 |