Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g01740 | A05 | 976510 | C | T | missense_variant | MODERATE | c.694G>A|p.Gly232Ser |
S20 |
2 | BAA05g01740 | A05 | 976554 | C | T | missense_variant | MODERATE | c.650G>A|p.Arg217Lys |
S291 |
3 | BAA05g01740 | A05 | 976663 | C | T | missense_variant | MODERATE | c.541G>A|p.Glu181Lys |
S50 |
4 | BAA05g01740 | A05 | 976727 | C | T | intron_variant | MODIFIER | c.513+34G>A| |
S268 |
5 | BAA05g01740 | A05 | 976791 | G | A | synonymous_variant | LOW | c.483C>T|p.Cys161Cys |
S179 |
6 | BAA05g01740 | A05 | 978169 | C | T | upstream_gene_variant | MODIFIER | c.-554G>A| |
S57 |
7 | BAA05g01740 | A05 | 978595 | G | A | upstream_gene_variant | MODIFIER | c.-980C>T| |
S280 |
8 | BAA05g01740 | A05 | 979437 | C | T | upstream_gene_variant | MODIFIER | c.-1822G>A| |
S36 |
9 | BAA05g01740 | A05 | 980856 | G | A | upstream_gene_variant | MODIFIER | c.-3241C>T| |
S190 |
10 | BAA05g01740 | A05 | 981214 | C | T | upstream_gene_variant | MODIFIER | c.-3599G>A| |
S271 |
11 | BAA05g01740 | A05 | 981664 | G | A | upstream_gene_variant | MODIFIER | c.-4049C>T| |
S294 |
12 | BAA05g01740 | A05 | 981816 | C | T | upstream_gene_variant | MODIFIER | c.-4201G>A| |
S153 S213 |