Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g14690 | A02 | 6857597 | G | A | upstream_gene_variant | MODIFIER | c.-1311G>A| |
S129 |
2 | BAA02g14690 | A02 | 6857754 | G | A | upstream_gene_variant | MODIFIER | c.-1154G>A| |
S69 |
3 | BAA02g14690 | A02 | 6857819 | G | A | upstream_gene_variant | MODIFIER | c.-1089G>A| |
S45 |
4 | BAA02g14690 | A02 | 6858151 | A | C | upstream_gene_variant | MODIFIER | c.-757A>C| |
S199 |
5 | BAA02g14690 | A02 | 6859848 | G | A | splice_region_variant&intron_variant | LOW | c.204-7G>A| |
S168 |
6 | BAA02g14690 | A02 | 6860038 | C | T | synonymous_variant | LOW | c.387C>T|p.Leu129Leu |
S276 |
7 | BAA02g14690 | A02 | 6860306 | G | A | missense_variant | MODERATE | c.655G>A|p.Ala219Thr |
S170 S207 |
8 | BAA02g14690 | A02 | 6860378 | G | A | missense_variant | MODERATE | c.727G>A|p.Asp243Asn |
S177 |
9 | BAA02g14690 | A02 | 6863913 | C | T | intron_variant | MODIFIER | c.1415-400C>T| |
S13 |
10 | BAA02g14690 | A02 | 6864057 | C | T | intron_variant | MODIFIER | c.1415-256C>T| |
S162 |
11 | BAA02g14690 | A02 | 6864203 | C | T | intron_variant | MODIFIER | c.1415-110C>T| |
S18 |
12 | BAA02g14690 | A02 | 6864480 | C | T | downstream_gene_variant | MODIFIER | c.*82C>T| |
S58 |
13 | BAA02g14690 | A02 | 6864488 | G | A | downstream_gene_variant | MODIFIER | c.*90G>A| |
S303 |
14 | BAA02g14690 | A02 | 6865161 | G | A | downstream_gene_variant | MODIFIER | c.*763G>A| |
S59 |
15 | BAA02g14690 | A02 | 6865909 | C | T | downstream_gene_variant | MODIFIER | c.*1511C>T| |
S268 |
16 | BAA02g14690 | A02 | 6866359 | C | T | downstream_gene_variant | MODIFIER | c.*1961C>T| |
S306 |