Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18790 | A10 | 17481954 | G | A | upstream_gene_variant | MODIFIER | c.-4671G>A| |
S65 |
2 | BAA10g18790 | A10 | 17482664 | C | T | upstream_gene_variant | MODIFIER | c.-3961C>T| |
S202 |
3 | BAA10g18790 | A10 | 17483204 | C | T | upstream_gene_variant | MODIFIER | c.-3421C>T| |
S51 |
4 | BAA10g18790 | A10 | 17483879 | G | A | upstream_gene_variant | MODIFIER | c.-2746G>A| |
S240 |
5 | BAA10g18790 | A10 | 17484326 | C | T | upstream_gene_variant | MODIFIER | c.-2299C>T| |
S301 S304 |
6 | BAA10g18790 | A10 | 17485301 | G | C | upstream_gene_variant | MODIFIER | c.-1324G>C| |
S49 |
7 | BAA10g18790 | A10 | 17485400 | G | A | upstream_gene_variant | MODIFIER | c.-1225G>A| |
S205 |
8 | BAA10g18790 | A10 | 17485644 | G | A | upstream_gene_variant | MODIFIER | c.-981G>A| |
S192 |
9 | BAA10g18790 | A10 | 17485885 | G | A | upstream_gene_variant | MODIFIER | c.-740G>A| |
S206 |
10 | BAA10g18790 | A10 | 17487254 | G | A | synonymous_variant | LOW | c.630G>A|p.Gly210Gly |
S250 |
11 | BAA10g18790 | A10 | 17487270 | G | A | missense_variant | MODERATE | c.646G>A|p.Glu216Lys |
S151 S263 |
12 | BAA10g18790 | A10 | 17487662 | G | A | stop_gained | HIGH | c.1038G>A|p.Trp346* |
S295 |