Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37170 | A02 | 31832867 | G | A | upstream_gene_variant | MODIFIER | c.-4501G>A| |
S110 |
2 | BAA02g37170 | A02 | 31834370 | G | A | upstream_gene_variant | MODIFIER | c.-2998G>A| |
S50 |
3 | BAA02g37170 | A02 | 31835244 | G | A | upstream_gene_variant | MODIFIER | c.-2124G>A| |
S272 |
4 | BAA02g37170 | A02 | 31835246 | C | T | upstream_gene_variant | MODIFIER | c.-2122C>T| |
S15 |
5 | BAA02g37170 | A02 | 31836204 | C | T | upstream_gene_variant | MODIFIER | c.-1164C>T| |
S262 |
6 | BAA02g37170 | A02 | 31836891 | C | T | upstream_gene_variant | MODIFIER | c.-477C>T| |
S268 |
7 | BAA02g37170 | A02 | 31837210 | C | T | upstream_gene_variant | MODIFIER | c.-158C>T| |
S240 |
8 | BAA02g37170 | A02 | 31837650 | C | T | intron_variant | MODIFIER | c.175+108C>T| |
S139 |
9 | BAA02g37170 | A02 | 31837655 | C | T | intron_variant | MODIFIER | c.175+113C>T| |
S114 |
10 | BAA02g37170 | A02 | 31837985 | C | T | intron_variant | MODIFIER | c.176-32C>T| |
S211 |
11 | BAA02g37170 | A02 | 31839018 | G | A | intron_variant | MODIFIER | c.555+81G>A| |
S76 |
12 | BAA02g37170 | A02 | 31840614 | C | T | downstream_gene_variant | MODIFIER | c.*1216C>T| |
S202 |
13 | BAA02g37170 | A02 | 31840869 | G | A | downstream_gene_variant | MODIFIER | c.*1471G>A| |
S279 |
14 | BAA02g37170 | A02 | 31841327 | G | A | downstream_gene_variant | MODIFIER | c.*1929G>A| |
S223 |
15 | BAA02g37170 | A02 | 31842493 | G | A | downstream_gene_variant | MODIFIER | c.*3095G>A| |
S23 |
16 | BAA02g37170 | A02 | 31842538 | C | T | downstream_gene_variant | MODIFIER | c.*3140C>T| |
S15 S3 |
17 | BAA02g37170 | A02 | 31842778 | T | C | downstream_gene_variant | MODIFIER | c.*3380T>C| |
S236 |