Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g17050 | A02 | 8482715 | C | T | upstream_gene_variant | MODIFIER | c.-4760C>T| |
S163 |
2 | BAA02g17050 | A02 | 8482915 | C | T | upstream_gene_variant | MODIFIER | c.-4560C>T| |
S264 |
3 | BAA02g17050 | A02 | 8484053 | G | A | upstream_gene_variant | MODIFIER | c.-3422G>A| |
S238 |
4 | BAA02g17050 | A02 | 8485813 | A | G | upstream_gene_variant | MODIFIER | c.-1662A>G| |
S206 |
5 | BAA02g17050 | A02 | 8485914 | C | T | upstream_gene_variant | MODIFIER | c.-1561C>T| |
S77 S82 |
6 | BAA02g17050 | A02 | 8486063 | G | A | upstream_gene_variant | MODIFIER | c.-1412G>A| |
S247 |
7 | BAA02g17050 | A02 | 8486201 | G | A | upstream_gene_variant | MODIFIER | c.-1274G>A| |
S35 |
8 | BAA02g17050 | A02 | 8486382 | G | A | upstream_gene_variant | MODIFIER | c.-1093G>A| |
S148 S30 S31 |
9 | BAA02g17050 | A02 | 8486983 | G | A | upstream_gene_variant | MODIFIER | c.-492G>A| |
S155 S211 |
10 | BAA02g17050 | A02 | 8488381 | G | A | missense_variant | MODERATE | c.655G>A|p.Gly219Ser |
S251 S66 |
11 | BAA02g17050 | A02 | 8489285 | C | T | synonymous_variant | LOW | c.1284C>T|p.Thr428Thr |
S70 |
12 | BAA02g17050 | A02 | 8489522 | G | A | intron_variant | MODIFIER | c.1429-57G>A| |
S174 S27 |
13 | BAA02g17050 | A02 | 8489684 | G | A | missense_variant | MODERATE | c.1534G>A|p.Asp512Asn |
S60 |
14 | BAA02g17050 | A02 | 8491485 | C | A | downstream_gene_variant | MODIFIER | c.*870C>A| |
S194 |