Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27950 | A02 | 15745095 | C | T | upstream_gene_variant | MODIFIER | c.-4655C>T| |
S286 |
2 | BAA02g27950 | A02 | 15745750 | C | T | upstream_gene_variant | MODIFIER | c.-4000C>T| |
S51 |
3 | BAA02g27950 | A02 | 15746431 | C | T | upstream_gene_variant | MODIFIER | c.-3319C>T| |
S178 |
4 | BAA02g27950 | A02 | 15747696 | C | T | upstream_gene_variant | MODIFIER | c.-2054C>T| |
S8 |
5 | BAA02g27950 | A02 | 15747756 | C | T | upstream_gene_variant | MODIFIER | c.-1994C>T| |
S219 |
6 | BAA02g27950 | A02 | 15747812 | C | T | upstream_gene_variant | MODIFIER | c.-1938C>T| |
S32 |
7 | BAA02g27950 | A02 | 15748580 | G | A | upstream_gene_variant | MODIFIER | c.-1170G>A| |
S174 S216 S27 |
8 | BAA02g27950 | A02 | 15748642 | A | T | upstream_gene_variant | MODIFIER | c.-1108A>T| |
S272 |
9 | BAA02g27950 | A02 | 15749805 | G | A | missense_variant | MODERATE | c.56G>A|p.Arg19Lys |
S38 |
10 | BAA02g27950 | A02 | 15749864 | C | T | stop_gained | HIGH | c.115C>T|p.Gln39* |
S264 |
11 | BAA02g27950 | A02 | 15750724 | C | T | missense_variant | MODERATE | c.554C>T|p.Ser185Phe |
S181 |
12 | BAA02g27950 | A02 | 15751412 | C | T | synonymous_variant | LOW | c.1242C>T|p.Gly414Gly |
S49 |
13 | BAA02g27950 | A02 | 15751565 | G | A | splice_region_variant&intron_variant | LOW | c.1324-6G>A| |
S148 S30 S31 |
14 | BAA02g27950 | A02 | 15751629 | G | A | missense_variant | MODERATE | c.1382G>A|p.Gly461Glu |
S81 |