Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g56150 | A03 | 27761004 | C | T | missense_variant | MODERATE | c.5263G>A|p.Glu1755Lys |
S184 |
2 | BAA03g56150 | A03 | 27761674 | C | T | synonymous_variant | LOW | c.4593G>A|p.Lys1531Lys |
S126 |
3 | BAA03g56150 | A03 | 27762063 | C | T | missense_variant | MODERATE | c.4204G>A|p.Val1402Ile |
S255 |
4 | BAA03g56150 | A03 | 27762153 | C | T | missense_variant | MODERATE | c.4114G>A|p.Val1372Met |
S293 |
5 | BAA03g56150 | A03 | 27762317 | G | A | missense_variant | MODERATE | c.3950C>T|p.Ser1317Phe |
S153 S213 |
6 | BAA03g56150 | A03 | 27762563 | C | T | missense_variant | MODERATE | c.3704G>A|p.Gly1235Glu |
S205 |
7 | BAA03g56150 | A03 | 27762604 | C | T | synonymous_variant | LOW | c.3663G>A|p.Lys1221Lys |
S243 |
8 | BAA03g56150 | A03 | 27763337 | G | A | synonymous_variant | LOW | c.3241C>T|p.Leu1081Leu |
S71 |
9 | BAA03g56150 | A03 | 27764989 | C | T | synonymous_variant | LOW | c.2487G>A|p.Gln829Gln |
S193 |
10 | BAA03g56150 | A03 | 27765822 | C | T | synonymous_variant | LOW | c.1965G>A|p.Gln655Gln |
S144 |
11 | BAA03g56150 | A03 | 27766052 | G | A | stop_gained | HIGH | c.1735C>T|p.Gln579* |
S95 |
12 | BAA03g56150 | A03 | 27767112 | G | A | missense_variant | MODERATE | c.949C>T|p.Pro317Ser |
S296 |
13 | BAA03g56150 | A03 | 27767274 | G | A | missense_variant | MODERATE | c.862C>T|p.His288Tyr |
S162 |
14 | BAA03g56150 | A03 | 27770649 | G | A | upstream_gene_variant | MODIFIER | c.-1810C>T| |
S177 |
15 | BAA03g56150 | A03 | 27772421 | G | A | upstream_gene_variant | MODIFIER | c.-3582C>T| |
S96 |
16 | BAA03g56150 | A03 | 27772539 | C | T | upstream_gene_variant | MODIFIER | c.-3700G>A| |
S155 S211 |
17 | BAA03g56150 | A03 | 27773363 | C | T | upstream_gene_variant | MODIFIER | c.-4524G>A| |
S163 |