Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g66890 | A03 | 41419249 | G | A | upstream_gene_variant | MODIFIER | c.-4710G>A| |
S169 |
2 | BAA03g66890 | A03 | 41419318 | G | A | upstream_gene_variant | MODIFIER | c.-4641G>A| |
S61 |
3 | BAA03g66890 | A03 | 41419646 | C | T | upstream_gene_variant | MODIFIER | c.-4313C>T| |
S200 |
4 | BAA03g66890 | A03 | 41419941 | G | A | upstream_gene_variant | MODIFIER | c.-4018G>A| |
S48 |
5 | BAA03g66890 | A03 | 41420569 | G | A | upstream_gene_variant | MODIFIER | c.-3390G>A| |
S298 |
6 | BAA03g66890 | A03 | 41420976 | C | T | upstream_gene_variant | MODIFIER | c.-2983C>T| |
S130 |
7 | BAA03g66890 | A03 | 41422144 | C | T | upstream_gene_variant | MODIFIER | c.-1815C>T| |
S252 |
8 | BAA03g66890 | A03 | 41424169 | G | A | intron_variant | MODIFIER | c.123+88G>A| |
S182 |
9 | BAA03g66890 | A03 | 41424366 | C | T | intron_variant | MODIFIER | c.124-67C>T| |
S251 |
10 | BAA03g66890 | A03 | 41424823 | C | T | missense_variant | MODERATE | c.392C>T|p.Thr131Ile |
S131 |
11 | BAA03g66890 | A03 | 41427657 | G | A | missense_variant | MODERATE | c.476G>A|p.Gly159Asp |
S181 |
12 | BAA03g66890 | A03 | 41427694 | C | T | synonymous_variant | LOW | c.513C>T|p.Ala171Ala |
S303 |
13 | BAA03g66890 | A03 | 41428822 | C | T | synonymous_variant | LOW | c.1092C>T|p.Leu364Leu |
S61 |
14 | BAA03g66890 | A03 | 41429300 | G | A | splice_region_variant&synonymous_variant | LOW | c.1314G>A|p.Gln438Gln |
S36 |
15 | BAA03g66890 | A03 | 41429774 | G | A | missense_variant | MODERATE | c.1703G>A|p.Gly568Glu |
S148 S210 S295 |
16 | BAA03g66890 | A03 | 41430138 | G | A | downstream_gene_variant | MODIFIER | c.*294G>A| |
S283 |