Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g10090 | A09 | 5563639 | C | T | missense_variant | MODERATE | c.1186G>A|p.Glu396Lys |
S171 |
2 | BAA09g10090 | A09 | 5563728 | C | T | missense_variant | MODERATE | c.1097G>A|p.Gly366Asp |
S279 |
3 | BAA09g10090 | A09 | 5563774 | C | T | missense_variant | MODERATE | c.1051G>A|p.Asp351Asn |
S35 |
4 | BAA09g10090 | A09 | 5563822 | G | A | missense_variant | MODERATE | c.1003C>T|p.Arg335Cys |
S260 |
5 | BAA09g10090 | A09 | 5563850 | C | T | synonymous_variant | LOW | c.975G>A|p.Glu325Glu |
S255 |
6 | BAA09g10090 | A09 | 5564145 | C | T | missense_variant | MODERATE | c.772G>A|p.Glu258Lys |
S277 |
7 | BAA09g10090 | A09 | 5564148 | C | T | missense_variant | MODERATE | c.769G>A|p.Glu257Lys |
S9 |
8 | BAA09g10090 | A09 | 5564195 | C | T | missense_variant | MODERATE | c.722G>A|p.Gly241Asp |
S9 |
9 | BAA09g10090 | A09 | 5564212 | G | A | synonymous_variant | LOW | c.705C>T|p.Thr235Thr |
S162 |
10 | BAA09g10090 | A09 | 5565760 | C | T | synonymous_variant | LOW | c.327G>A|p.Glu109Glu |
S156 |
11 | BAA09g10090 | A09 | 5565770 | G | A | missense_variant | MODERATE | c.317C>T|p.Ser106Leu |
S226 |
12 | BAA09g10090 | A09 | 5565925 | C | T | missense_variant | MODERATE | c.247G>A|p.Asp83Asn |
S246 |
13 | BAA09g10090 | A09 | 5566432 | G | A | missense_variant | MODERATE | c.49C>T|p.Arg17Cys |
S169 |
14 | BAA09g10090 | A09 | 5569895 | G | A | upstream_gene_variant | MODIFIER | c.-3415C>T| |
S95 |
15 | BAA09g10090 | A09 | 5570581 | C | T | upstream_gene_variant | MODIFIER | c.-4101G>A| |
S69 |
16 | BAA09g10090 | A09 | 5570612 | C | T | upstream_gene_variant | MODIFIER | c.-4132G>A| |
S115 |
17 | BAA09g10090 | A09 | 5570628 | C | T | upstream_gene_variant | MODIFIER | c.-4148G>A| |
S10 |