Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46150 | A02 | 37599544 | G | A | synonymous_variant | LOW | c.2832C>T|p.Ser944Ser |
S298 |
2 | BAA02g46150 | A02 | 37604493 | C | T | intron_variant | MODIFIER | c.1765-142G>A| |
S233 |
3 | BAA02g46150 | A02 | 37604963 | C | T | intron_variant | MODIFIER | c.1765-612G>A| |
S173 |
4 | BAA02g46150 | A02 | 37605397 | C | T | intron_variant | MODIFIER | c.1764+353G>A| |
S32 |
5 | BAA02g46150 | A02 | 37606927 | C | T | missense_variant | MODERATE | c.587G>A|p.Gly196Glu |
S142 |
6 | BAA02g46150 | A02 | 37607276 | C | T | intron_variant | MODIFIER | c.572-334G>A| |
S189 |
7 | BAA02g46150 | A02 | 37608078 | C | T | missense_variant | MODERATE | c.484G>A|p.Val162Met |
S259 |
8 | BAA02g46150 | A02 | 37608489 | C | T | intron_variant | MODIFIER | c.298-136G>A| |
S250 |
9 | BAA02g46150 | A02 | 37609870 | C | T | upstream_gene_variant | MODIFIER | c.-700G>A| |
S9 |
10 | BAA02g46150 | A02 | 37610037 | C | T | upstream_gene_variant | MODIFIER | c.-867G>A| |
S6 |
11 | BAA02g46150 | A02 | 37610636 | C | T | upstream_gene_variant | MODIFIER | c.-1466G>A| |
S124 |
12 | BAA02g46150 | A02 | 37611980 | C | T | upstream_gene_variant | MODIFIER | c.-2810G>A| |
S122 |
13 | BAA02g46150 | A02 | 37612488 | C | T | upstream_gene_variant | MODIFIER | c.-3318G>A| |
S115 |