Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
7051 | BAA01g05780 | A01 | 2574847 | A | C | missense_variant | MODERATE | c.172A>C|p.Ile58Leu |
S15 S156 S2 S3 S4 S6 |
7052 | BAA01g05780 | A01 | 2575126 | G | A | synonymous_variant | LOW | c.294G>A|p.Arg98Arg |
S127 |
7053 | BAA01g05780 | A01 | 2575201 | C | T | synonymous_variant | LOW | c.369C>T|p.Leu123Leu |
S94 |
7054 | BAA01g05780 | A01 | 2575480 | G | A | synonymous_variant | LOW | c.648G>A|p.Gly216Gly |
S257 |
7055 | BAA01g05780 | A01 | 2575557 | C | T | missense_variant | MODERATE | c.725C>T|p.Ala242Val |
S192 |
7056 | BAA01g05780 | A01 | 2575854 | G | A | missense_variant | MODERATE | c.931G>A|p.Asp311Asn |
S180 S268 |
7057 | BAA01g05780 | A01 | 2576358 | C | T | synonymous_variant | LOW | c.1362C>T|p.Pro454Pro |
S46 |
7058 | BAA01g05780 | A01 | 2576946 | C | T | synonymous_variant | LOW | c.1842C>T|p.Asp614Asp |
S119 |
7059 | BAA01g05780 | A01 | 2577640 | G | A | missense_variant | MODERATE | c.2282G>A|p.Gly761Glu |
S308 |
7060 | BAA01g05790 | A01 | 2579450 | C | T | missense_variant | MODERATE | c.706G>A|p.Asp236Asn |
S182 |
7061 | BAA01g05790 | A01 | 2579944 | G | A | synonymous_variant | LOW | c.492C>T|p.Ser164Ser |
S12 |
7062 | BAA01g05790 | A01 | 2580463 | C | T | synonymous_variant | LOW | c.312G>A|p.Lys104Lys |
S54 |
7063 | BAA01g05790 | A01 | 2581742 | G | A | upstream_gene_variant | MODIFIER | c.-554C>T| |
S107 |
7064 | BAA01g05790 | A01 | 2581856 | C | T | upstream_gene_variant | MODIFIER | c.-668G>A| |
S180 |
7065 | BAA01g05790 | A01 | 2581945 | G | A | upstream_gene_variant | MODIFIER | c.-757C>T| |
S39 |
7066 | BAA01g05800 | A01 | 2583843 | C | T | synonymous_variant | LOW | c.594C>T|p.Leu198Leu |
S68 |
7067 | BAA01g05790 | A01 | 2584138 | C | T | upstream_gene_variant | MODIFIER | c.-2950G>A| |
S167 |
7068 | BAA01g05800 | A01 | 2584370 | G | A | missense_variant | MODERATE | c.893G>A|p.Arg298His |
S140 |
7069 | BAA01g05790 | A01 | 2585004 | G | A | upstream_gene_variant | MODIFIER | c.-3816C>T| |
S136 |
7070 | BAA01g05800 | A01 | 2585069 | G | A | missense_variant&splice_region_variant | MODERATE | c.1246G>A|p.Val416Ile |
S161 |
7071 | BAA01g05800 | A01 | 2586100 | G | A | missense_variant | MODERATE | c.1726G>A|p.Glu576Lys |
S293 |
7072 | BAA01g05800 | A01 | 2586160 | G | A | missense_variant | MODERATE | c.1786G>A|p.Asp596Asn |
S202 |
7073 | BAA01g05800 | A01 | 2586718 | G | A | downstream_gene_variant | MODIFIER | c.*202G>A| |
S149 |
7074 | BAA01g05800 | A01 | 2586817 | G | A | downstream_gene_variant | MODIFIER | c.*301G>A| |
S293 |
7075 | BAA01g05800 | A01 | 2587288 | C | T | downstream_gene_variant | MODIFIER | c.*772C>T| |
S212 |