Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
6801 | BAA01g05590 | A01 | 2472126 | G | A | upstream_gene_variant | MODIFIER | c.-275C>T| |
S56 |
6802 | BAA01g05590 | A01 | 2472863 | C | T | upstream_gene_variant | MODIFIER | c.-1012G>A| |
S218 |
6803 | BAA01g05590 | A01 | 2473464 | G | A | upstream_gene_variant | MODIFIER | c.-1613C>T| |
S33 |
6804 | BAA01g05590 | A01 | 2473514 | G | T | upstream_gene_variant | MODIFIER | c.-1663C>A| |
S306 |
6805 | BAA01g05590 | A01 | 2473996 | C | T | upstream_gene_variant | MODIFIER | c.-2145G>A| |
S43 |
6806 | BAA01g05590 | A01 | 2474126 | G | A | upstream_gene_variant | MODIFIER | c.-2275C>T| |
S40 S49 |
6807 | BAA01g05600 | A01 | 2474484 | C | T | missense_variant | MODERATE | c.86C>T|p.Thr29Ile |
S44 |
6808 | BAA01g05590 | A01 | 2475536 | C | T | upstream_gene_variant | MODIFIER | c.-3685G>A| |
S150 |
6809 | BAA01g05600 | A01 | 2475636 | C | T | missense_variant | MODERATE | c.443C>T|p.Pro148Leu |
S74 |
6810 | BAA01g05590 | A01 | 2475778 | C | T | upstream_gene_variant | MODIFIER | c.-3927G>A| |
S48 |
6811 | BAA01g05600 | A01 | 2476389 | G | A | synonymous_variant | LOW | c.765G>A|p.Val255Val |
S159 S243 |
6812 | BAA01g05600 | A01 | 2476414 | C | T | synonymous_variant | LOW | c.790C>T|p.Leu264Leu |
S72 S78 |
6813 | BAA01g05600 | A01 | 2476718 | G | A | synonymous_variant | LOW | c.1014G>A|p.Ser338Ser |
S63 |
6814 | BAA01g05620 | A01 | 2477573 | C | T | upstream_gene_variant | MODIFIER | c.-3780C>T| |
S2 |
6815 | BAA01g05620 | A01 | 2478834 | G | A | upstream_gene_variant | MODIFIER | c.-2519G>A| |
S259 |
6816 | BAA01g05620 | A01 | 2479218 | C | T | upstream_gene_variant | MODIFIER | c.-2135C>T| |
S97 |
6817 | BAA01g05610 | A01 | 2479904 | C | T | upstream_gene_variant | MODIFIER | c.-173G>A| |
S35 |
6818 | BAA01g05610 | A01 | 2480629 | G | A | upstream_gene_variant | MODIFIER | c.-898C>T| |
S173 S176 |
6819 | BAA01g05620 | A01 | 2483597 | G | A | missense_variant | MODERATE | c.1616G>A|p.Arg539Lys |
S183 S198 |
6820 | BAA01g05620 | A01 | 2484000 | G | A | synonymous_variant | LOW | c.2019G>A|p.Glu673Glu |
S136 |
6821 | BAA01g05620 | A01 | 2484578 | C | T | missense_variant | MODERATE | c.2333C>T|p.Ser778Phe |
S18 |
6822 | BAA01g05620 | A01 | 2484637 | G | A | missense_variant | MODERATE | c.2392G>A|p.Gly798Arg |
S116 |
6823 | BAA01g05620 | A01 | 2485146 | G | A | missense_variant | MODERATE | c.2794G>A|p.Ala932Thr |
S201 |
6824 | BAA01g05620 | A01 | 2485247 | C | T | synonymous_variant | LOW | c.2895C>T|p.Tyr965Tyr |
S218 |
6825 | BAA01g05620 | A01 | 2485268 | C | T | synonymous_variant | LOW | c.2916C>T|p.His972His |
S54 |