Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g06390 | A05 | 3095238 | C | T | upstream_gene_variant | MODIFIER | c.-3825C>T| |
S169 |
2 | BAA05g06390 | A05 | 3095646 | C | T | upstream_gene_variant | MODIFIER | c.-3417C>T| |
S87 |
3 | BAA05g06390 | A05 | 3096780 | C | T | upstream_gene_variant | MODIFIER | c.-2283C>T| |
S107 |
4 | BAA05g06390 | A05 | 3098109 | C | T | upstream_gene_variant | MODIFIER | c.-954C>T| |
S97 |
5 | BAA05g06390 | A05 | 3098532 | C | T | upstream_gene_variant | MODIFIER | c.-531C>T| |
S295 |
6 | BAA05g06390 | A05 | 3098796 | G | A | upstream_gene_variant | MODIFIER | c.-267G>A| |
S252 |
7 | BAA05g06390 | A05 | 3098982 | C | A | upstream_gene_variant | MODIFIER | c.-81C>A| |
S32 |
8 | BAA05g06390 | A05 | 3099374 | G | A | synonymous_variant | LOW | c.312G>A|p.Glu104Glu |
S223 |
9 | BAA05g06390 | A05 | 3100512 | G | A | missense_variant | MODERATE | c.782G>A|p.Gly261Asp |
S221 |
10 | BAA05g06390 | A05 | 3101417 | C | T | synonymous_variant | LOW | c.1209C>T|p.Asn403Asn |
S13 |
11 | BAA05g06390 | A05 | 3101485 | G | A | missense_variant | MODERATE | c.1277G>A|p.Arg426Lys |
S217 |
12 | BAA05g06390 | A05 | 3101846 | G | A | missense_variant | MODERATE | c.1638G>A|p.Met546Ile |
S200 |
13 | BAA05g06390 | A05 | 3101878 | C | T | missense_variant | MODERATE | c.1670C>T|p.Pro557Leu |
S146 |
14 | BAA05g06390 | A05 | 3103525 | G | A | downstream_gene_variant | MODIFIER | c.*1505G>A| |
S231 |
15 | BAA05g06390 | A05 | 3104119 | C | T | downstream_gene_variant | MODIFIER | c.*2099C>T| |
S171 |
16 | BAA05g06390 | A05 | 3105635 | C | T | downstream_gene_variant | MODIFIER | c.*3615C>T| |
S207 |