Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g01730 | A06 | 1090964 | C | T | missense_variant | MODERATE | c.1517G>A|p.Arg506Lys |
S23 |
2 | BAA06g01730 | A06 | 1091093 | C | T | missense_variant | MODERATE | c.1388G>A|p.Gly463Glu |
S36 |
3 | BAA06g01730 | A06 | 1092382 | C | T | missense_variant&splice_region_variant | MODERATE | c.628G>A|p.Val210Ile |
S279 |
4 | BAA06g01730 | A06 | 1092559 | G | A | missense_variant | MODERATE | c.535C>T|p.Leu179Phe |
S140 |
5 | BAA06g01730 | A06 | 1093255 | C | T | synonymous_variant | LOW | c.420G>A|p.Gly140Gly |
S219 S72 |
6 | BAA06g01730 | A06 | 1093589 | C | T | missense_variant | MODERATE | c.332G>A|p.Arg111Lys |
S288 |
7 | BAA06g01730 | A06 | 1093591 | C | T | synonymous_variant | LOW | c.330G>A|p.Glu110Glu |
S161 |
8 | BAA06g01730 | A06 | 1093671 | C | T | missense_variant | MODERATE | c.250G>A|p.Val84Met |
S80 |
9 | BAA06g01730 | A06 | 1093785 | G | A | synonymous_variant | LOW | c.201C>T|p.Pro67Pro |
S47 |
10 | BAA06g01730 | A06 | 1093842 | G | A | synonymous_variant | LOW | c.144C>T|p.Pro48Pro |
S244 |
11 | BAA06g01730 | A06 | 1093920 | G | A | synonymous_variant | LOW | c.66C>T|p.Arg22Arg |
S180 |
12 | BAA06g01730 | A06 | 1094499 | G | A | upstream_gene_variant | MODIFIER | c.-514C>T| |
S233 |
13 | BAA06g01730 | A06 | 1095683 | G | A | upstream_gene_variant | MODIFIER | c.-1698C>T| |
S115 |
14 | BAA06g01730 | A06 | 1097614 | G | A | upstream_gene_variant | MODIFIER | c.-3629C>T| |
S291 |