Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g20550 | A06 | 10903568 | C | T | upstream_gene_variant | MODIFIER | c.-4248C>T| |
S279 |
2 | BAA06g20550 | A06 | 10904628 | C | T | upstream_gene_variant | MODIFIER | c.-3188C>T| |
S257 |
3 | BAA06g20550 | A06 | 10906336 | G | A | upstream_gene_variant | MODIFIER | c.-1480G>A| |
S173 |
4 | BAA06g20550 | A06 | 10906396 | T | A | upstream_gene_variant | MODIFIER | c.-1420T>A| |
S204 |
5 | BAA06g20550 | A06 | 10906659 | C | T | upstream_gene_variant | MODIFIER | c.-1157C>T| |
S4 |
6 | BAA06g20550 | A06 | 10907283 | G | A | upstream_gene_variant | MODIFIER | c.-533G>A| |
S177 |
7 | BAA06g20550 | A06 | 10907555 | G | A | upstream_gene_variant | MODIFIER | c.-261G>A| |
S184 |
8 | BAA06g20550 | A06 | 10908765 | C | T | missense_variant | MODERATE | c.83C>T|p.Pro28Leu |
S196 |
9 | BAA06g20550 | A06 | 10909163 | C | T | missense_variant | MODERATE | c.440C>T|p.Ala147Val |
S60 |
10 | BAA06g20550 | A06 | 10909273 | G | A | missense_variant | MODERATE | c.550G>A|p.Asp184Asn |
S226 |
11 | BAA06g20550 | A06 | 10909341 | G | A | synonymous_variant | LOW | c.618G>A|p.Lys206Lys |
S105 S106 |
12 | BAA06g20550 | A06 | 10909353 | G | A | synonymous_variant | LOW | c.630G>A|p.Lys210Lys |
S95 |