Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g41060 | A06 | 26758778 | C | T | upstream_gene_variant | MODIFIER | c.-4760C>T| |
S25 |
2 | BAA06g41060 | A06 | 26759629 | G | A | upstream_gene_variant | MODIFIER | c.-3909G>A| |
S12 |
3 | BAA06g41060 | A06 | 26761177 | C | T | upstream_gene_variant | MODIFIER | c.-2361C>T| |
S18 |
4 | BAA06g41060 | A06 | 26761514 | C | T | upstream_gene_variant | MODIFIER | c.-2024C>T| |
S295 |
5 | BAA06g41060 | A06 | 26761665 | G | A | upstream_gene_variant | MODIFIER | c.-1873G>A| |
S51 |
6 | BAA06g41060 | A06 | 26762003 | G | A | upstream_gene_variant | MODIFIER | c.-1535G>A| |
S20 |
7 | BAA06g41060 | A06 | 26762647 | G | A | upstream_gene_variant | MODIFIER | c.-891G>A| |
S211 |
8 | BAA06g41060 | A06 | 26763406 | C | T | upstream_gene_variant | MODIFIER | c.-132C>T| |
S196 |
9 | BAA06g41060 | A06 | 26763904 | C | T | synonymous_variant | LOW | c.189C>T|p.Thr63Thr |
S69 |
10 | BAA06g41060 | A06 | 26763944 | C | T | missense_variant | MODERATE | c.229C>T|p.Leu77Phe |
S89 |
11 | BAA06g41060 | A06 | 26763955 | C | T | synonymous_variant | LOW | c.240C>T|p.Gly80Gly |
S134 |
12 | BAA06g41060 | A06 | 26764359 | C | T | missense_variant | MODERATE | c.560C>T|p.Ser187Phe |
S272 |
13 | BAA06g41060 | A06 | 26764914 | C | T | downstream_gene_variant | MODIFIER | c.*353C>T| |
S167 |
14 | BAA06g41060 | A06 | 26766751 | G | A | downstream_gene_variant | MODIFIER | c.*2190G>A| |
S251 |
15 | BAA06g41060 | A06 | 26767162 | G | A | downstream_gene_variant | MODIFIER | c.*2601G>A| |
S59 |
16 | BAA06g41060 | A06 | 26767291 | G | A | downstream_gene_variant | MODIFIER | c.*2730G>A| |
S126 |