Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g21850 | A02 | 11760413 | G | A | upstream_gene_variant | MODIFIER | c.-4442G>A| |
S174 S27 |
2 | BAA02g21850 | A02 | 11760555 | G | A | upstream_gene_variant | MODIFIER | c.-4300G>A| |
S86 |
3 | BAA02g21850 | A02 | 11760643 | G | A | upstream_gene_variant | MODIFIER | c.-4212G>A| |
S161 |
4 | BAA02g21850 | A02 | 11760892 | C | T | upstream_gene_variant | MODIFIER | c.-3963C>T| |
S107 |
5 | BAA02g21850 | A02 | 11761647 | C | T | upstream_gene_variant | MODIFIER | c.-3208C>T| |
S234 |
6 | BAA02g21850 | A02 | 11762349 | G | T | upstream_gene_variant | MODIFIER | c.-2506G>T| |
S188 |
7 | BAA02g21850 | A02 | 11762522 | C | T | upstream_gene_variant | MODIFIER | c.-2333C>T| |
S42 |
8 | BAA02g21850 | A02 | 11762727 | C | T | upstream_gene_variant | MODIFIER | c.-2128C>T| |
S183 S198 |
9 | BAA02g21850 | A02 | 11763997 | G | A | upstream_gene_variant | MODIFIER | c.-858G>A| |
S48 |
10 | BAA02g21850 | A02 | 11764391 | C | T | upstream_gene_variant | MODIFIER | c.-464C>T| |
S224 |
11 | BAA02g21850 | A02 | 11765349 | G | A | missense_variant | MODERATE | c.416G>A|p.Ser139Asn |
S68 |
12 | BAA02g21850 | A02 | 11765861 | G | A | missense_variant | MODERATE | c.928G>A|p.Glu310Lys |
S126 |
13 | BAA02g21850 | A02 | 11766958 | G | A | missense_variant | MODERATE | c.1739G>A|p.Arg580Lys |
S295 |
14 | BAA02g21850 | A02 | 11767648 | G | A | missense_variant | MODERATE | c.2429G>A|p.Gly810Glu |
S278 |
15 | BAA02g21850 | A02 | 11768607 | C | T | missense_variant | MODERATE | c.3146C>T|p.Ser1049Phe |
S5 |
16 | BAA02g21850 | A02 | 11768950 | G | A | synonymous_variant | LOW | c.3489G>A|p.Arg1163Arg |
S111 |
17 | BAA02g21850 | A02 | 11769111 | C | T | missense_variant | MODERATE | c.3650C>T|p.Thr1217Ile |
S255 |
18 | BAA02g21850 | A02 | 11770762 | G | A | downstream_gene_variant | MODIFIER | c.*515G>A| |
S204 |
19 | BAA02g21850 | A02 | 11770998 | G | A | downstream_gene_variant | MODIFIER | c.*751G>A| |
S295 |
20 | BAA02g21850 | A02 | 11773684 | C | T | downstream_gene_variant | MODIFIER | c.*3437C>T| |
S266 |