Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g33190 | A09 | 41843468 | C | T | downstream_gene_variant | MODIFIER | c.*1660G>A| |
S208 S219 |
2 | BAA09g33190 | A09 | 41844716 | C | T | downstream_gene_variant | MODIFIER | c.*412G>A| |
S246 |
3 | BAA09g33190 | A09 | 41844910 | G | A | downstream_gene_variant | MODIFIER | c.*218C>T| |
S62 |
4 | BAA09g33190 | A09 | 41845216 | C | T | missense_variant | MODERATE | c.536G>A|p.Ser179Asn |
S294 |
5 | BAA09g33190 | A09 | 41845405 | G | A | missense_variant | MODERATE | c.445C>T|p.His149Tyr |
S136 |
6 | BAA09g33190 | A09 | 41845582 | C | T | missense_variant | MODERATE | c.268G>A|p.Val90Ile |
S51 |
7 | BAA09g33190 | A09 | 41846104 | G | A | intron_variant | MODIFIER | c.131-385C>T| |
S85 |
8 | BAA09g33190 | A09 | 41846272 | G | A | intron_variant | MODIFIER | c.131-553C>T| |
S78 S83 |
9 | BAA09g33190 | A09 | 41846518 | C | T | intron_variant | MODIFIER | c.130+491G>A| |
S90 |
10 | BAA09g33190 | A09 | 41847177 | C | T | upstream_gene_variant | MODIFIER | c.-39G>A| |
S245 |
11 | BAA09g33190 | A09 | 41848322 | C | T | upstream_gene_variant | MODIFIER | c.-1184G>A| |
S36 |
12 | BAA09g33190 | A09 | 41849658 | G | A | upstream_gene_variant | MODIFIER | c.-2520C>T| |
S174 S216 S27 S39 |
13 | BAA09g33190 | A09 | 41849850 | C | T | upstream_gene_variant | MODIFIER | c.-2712G>A| |
S240 |
14 | BAA09g33190 | A09 | 41850214 | C | T | upstream_gene_variant | MODIFIER | c.-3076G>A| |
S246 |
15 | BAA09g33190 | A09 | 41851013 | G | A | upstream_gene_variant | MODIFIER | c.-3875C>T| |
S196 |
16 | BAA09g33190 | A09 | 41851554 | C | T | upstream_gene_variant | MODIFIER | c.-4416G>A| |
S279 |
17 | BAA09g33190 | A09 | 41852033 | C | T | upstream_gene_variant | MODIFIER | c.-4895G>A| |
S278 |
18 | BAA09g33190 | A09 | 41852098 | C | T | upstream_gene_variant | MODIFIER | c.-4960G>A| |
S19 |