Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11620 | A02 | 5252269 | C | T | upstream_gene_variant | MODIFIER | c.-1394C>T| |
S283 |
2 | BAA02g11620 | A02 | 5252447 | G | A | upstream_gene_variant | MODIFIER | c.-1216G>A| |
S192 |
3 | BAA02g11620 | A02 | 5253294 | C | T | upstream_gene_variant | MODIFIER | c.-369C>T| |
S157 S163 |
4 | BAA02g11620 | A02 | 5253992 | C | T | synonymous_variant | LOW | c.330C>T|p.Asn110Asn |
S299 |
5 | BAA02g11620 | A02 | 5254052 | C | T | synonymous_variant | LOW | c.390C>T|p.Phe130Phe |
S51 |
6 | BAA02g11620 | A02 | 5254370 | G | A | synonymous_variant | LOW | c.708G>A|p.Arg236Arg |
S57 |
7 | BAA02g11620 | A02 | 5254875 | G | A | missense_variant | MODERATE | c.1213G>A|p.Glu405Lys |
S107 |
8 | BAA02g11620 | A02 | 5254923 | C | T | missense_variant | MODERATE | c.1261C>T|p.Leu421Phe |
S194 |
9 | BAA02g11620 | A02 | 5255116 | A | C | missense_variant | MODERATE | c.1454A>C|p.Lys485Thr |
S150 S240 S67 |
10 | BAA02g11620 | A02 | 5255190 | G | A | missense_variant | MODERATE | c.1528G>A|p.Glu510Lys |
S52 |
11 | BAA02g11620 | A02 | 5255274 | G | A | missense_variant | MODERATE | c.1612G>A|p.Asp538Asn |
S143 |
12 | BAA02g11620 | A02 | 5255637 | G | A | downstream_gene_variant | MODIFIER | c.*115G>A| |
S158 |
13 | BAA02g11620 | A02 | 5255839 | G | A | downstream_gene_variant | MODIFIER | c.*317G>A| |
S271 |
14 | BAA02g11620 | A02 | 5256259 | A | G | downstream_gene_variant | MODIFIER | c.*737A>G| |
S216 |
15 | BAA02g11620 | A02 | 5256420 | G | A | downstream_gene_variant | MODIFIER | c.*898G>A| |
S20 |
16 | BAA02g11620 | A02 | 5256955 | G | A | downstream_gene_variant | MODIFIER | c.*1433G>A| |
S221 |