Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g14570 | A05 | 7675943 | C | T | upstream_gene_variant | MODIFIER | c.-3850C>T| |
S50 |
2 | BAA05g14570 | A05 | 7676056 | G | A | upstream_gene_variant | MODIFIER | c.-3737G>A| |
S244 |
3 | BAA05g14570 | A05 | 7676321 | G | A | upstream_gene_variant | MODIFIER | c.-3472G>A| |
S293 |
4 | BAA05g14570 | A05 | 7676956 | C | T | upstream_gene_variant | MODIFIER | c.-2837C>T| |
S184 |
5 | BAA05g14570 | A05 | 7677444 | C | T | upstream_gene_variant | MODIFIER | c.-2349C>T| |
S44 |
6 | BAA05g14570 | A05 | 7678795 | G | A | upstream_gene_variant | MODIFIER | c.-998G>A| |
S173 |
7 | BAA05g14570 | A05 | 7679696 | C | T | upstream_gene_variant | MODIFIER | c.-97C>T| |
S130 |
8 | BAA05g14570 | A05 | 7680476 | G | A | missense_variant | MODERATE | c.430G>A|p.Val144Ile |
S272 |
9 | BAA05g14570 | A05 | 7680727 | C | T | synonymous_variant | LOW | c.681C>T|p.Phe227Phe |
S115 |
10 | BAA05g14570 | A05 | 7680982 | C | T | intron_variant | MODIFIER | c.870-14C>T| |
S261 |
11 | BAA05g14570 | A05 | 7681159 | G | A | missense_variant | MODERATE | c.1033G>A|p.Glu345Lys |
S224 |
12 | BAA05g14570 | A05 | 7681176 | C | T | synonymous_variant | LOW | c.1050C>T|p.Phe350Phe |
S267 |
13 | BAA05g14570 | A05 | 7683578 | G | A | downstream_gene_variant | MODIFIER | c.*763G>A| |
S245 |
14 | BAA05g14570 | A05 | 7683814 | C | T | downstream_gene_variant | MODIFIER | c.*999C>T| |
S44 |
15 | BAA05g14570 | A05 | 7683906 | C | T | downstream_gene_variant | MODIFIER | c.*1091C>T| |
S36 |
16 | BAA05g14570 | A05 | 7684484 | G | A | downstream_gene_variant | MODIFIER | c.*1669G>A| |
S187 |
17 | BAA05g14570 | A05 | 7684760 | C | T | downstream_gene_variant | MODIFIER | c.*1945C>T| |
S36 |
18 | BAA05g14570 | A05 | 7685825 | G | A | downstream_gene_variant | MODIFIER | c.*3010G>A| |
S261 |
19 | BAA05g14570 | A05 | 7687719 | G | A | downstream_gene_variant | MODIFIER | c.*4904G>A| |
S124 |