Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g54610 | A03 | 26960328 | C | T | missense_variant&splice_region_variant | MODERATE | c.3251G>A|p.Arg1084Lys |
S229 |
2 | BAA03g54610 | A03 | 26961119 | C | T | missense_variant | MODERATE | c.2614G>A|p.Glu872Lys |
S262 |
3 | BAA03g54610 | A03 | 26961391 | C | T | missense_variant | MODERATE | c.2426G>A|p.Cys809Tyr |
S34 |
4 | BAA03g54610 | A03 | 26961595 | C | T | missense_variant | MODERATE | c.2315G>A|p.Ser772Asn |
S117 |
5 | BAA03g54610 | A03 | 26962342 | C | T | missense_variant | MODERATE | c.1936G>A|p.Asp646Asn |
S200 |
6 | BAA03g54610 | A03 | 26963166 | C | T | splice_region_variant&intron_variant | LOW | c.1635+3G>A| |
S180 |
7 | BAA03g54610 | A03 | 26963899 | G | A | synonymous_variant | LOW | c.1227C>T|p.Arg409Arg |
S292 |
8 | BAA03g54610 | A03 | 26964691 | C | T | missense_variant | MODERATE | c.788G>A|p.Gly263Asp |
S139 |
9 | BAA03g54610 | A03 | 26964981 | C | T | synonymous_variant | LOW | c.498G>A|p.Arg166Arg |
S44 |
10 | BAA03g54610 | A03 | 26965389 | C | T | synonymous_variant | LOW | c.90G>A|p.Pro30Pro |
S121 |
11 | BAA03g54610 | A03 | 26965411 | G | A | missense_variant | MODERATE | c.68C>T|p.Pro23Leu |
S269 |
12 | BAA03g54610 | A03 | 26966119 | G | A | upstream_gene_variant | MODIFIER | c.-641C>T| |
S168 |
13 | BAA03g54610 | A03 | 26966519 | G | A | upstream_gene_variant | MODIFIER | c.-1041C>T| |
S236 |
14 | BAA03g54610 | A03 | 26966609 | G | A | upstream_gene_variant | MODIFIER | c.-1131C>T| |
S86 |
15 | BAA03g54610 | A03 | 26968513 | C | T | upstream_gene_variant | MODIFIER | c.-3035G>A| |
S2 |
16 | BAA03g54610 | A03 | 26968840 | C | T | upstream_gene_variant | MODIFIER | c.-3362G>A| |
S67 |