Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g14600 | A03 | 6038207 | C | T | missense_variant | MODERATE | c.745G>A|p.Ala249Thr |
S272 |
2 | BAA03g14600 | A03 | 6038241 | G | A | synonymous_variant | LOW | c.711C>T|p.Asn237Asn |
S10 |
3 | BAA03g14600 | A03 | 6038604 | G | A | synonymous_variant | LOW | c.348C>T|p.Ala116Ala |
S206 S26 |
4 | BAA03g14600 | A03 | 6038676 | C | T | synonymous_variant | LOW | c.276G>A|p.Gln92Gln |
S123 |
5 | BAA03g14600 | A03 | 6038841 | G | A | synonymous_variant | LOW | c.111C>T|p.Asn37Asn |
S230 |
6 | BAA03g14600 | A03 | 6038855 | G | A | missense_variant | MODERATE | c.97C>T|p.Arg33Trp |
S162 |
7 | BAA03g14600 | A03 | 6039557 | G | A | upstream_gene_variant | MODIFIER | c.-522C>T| |
S289 S290 |
8 | BAA03g14600 | A03 | 6039980 | C | T | upstream_gene_variant | MODIFIER | c.-945G>A| |
S19 |
9 | BAA03g14600 | A03 | 6040856 | C | T | upstream_gene_variant | MODIFIER | c.-1821G>A| |
S229 |
10 | BAA03g14600 | A03 | 6041491 | C | T | upstream_gene_variant | MODIFIER | c.-2456G>A| |
S157 S163 |
11 | BAA03g14600 | A03 | 6041835 | C | T | upstream_gene_variant | MODIFIER | c.-2800G>A| |
S132 S137 |
12 | BAA03g14600 | A03 | 6042638 | C | T | upstream_gene_variant | MODIFIER | c.-3603G>A| |
S32 |
13 | BAA03g14600 | A03 | 6043286 | G | A | upstream_gene_variant | MODIFIER | c.-4251C>T| |
S228 |
14 | BAA03g14600 | A03 | 6043428 | G | A | upstream_gene_variant | MODIFIER | c.-4393C>T| |
S262 |