Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g03260 | A08 | 2264955 | C | T | upstream_gene_variant | MODIFIER | c.-4724C>T| |
S80 |
2 | BAA08g03260 | A08 | 2265257 | G | A | upstream_gene_variant | MODIFIER | c.-4422G>A| |
S247 |
3 | BAA08g03260 | A08 | 2265708 | G | A | upstream_gene_variant | MODIFIER | c.-3971G>A| |
S121 |
4 | BAA08g03260 | A08 | 2265824 | G | A | upstream_gene_variant | MODIFIER | c.-3855G>A| |
S278 |
5 | BAA08g03260 | A08 | 2265937 | C | T | upstream_gene_variant | MODIFIER | c.-3742C>T| |
S292 |
6 | BAA08g03260 | A08 | 2266095 | G | A | upstream_gene_variant | MODIFIER | c.-3584G>A| |
S124 |
7 | BAA08g03260 | A08 | 2266256 | C | T | upstream_gene_variant | MODIFIER | c.-3423C>T| |
S38 |
8 | BAA08g03260 | A08 | 2266390 | C | T | upstream_gene_variant | MODIFIER | c.-3289C>T| |
S308 |
9 | BAA08g03260 | A08 | 2266420 | G | A | upstream_gene_variant | MODIFIER | c.-3259G>A| |
S13 |
10 | BAA08g03260 | A08 | 2269102 | G | A | upstream_gene_variant | MODIFIER | c.-577G>A| |
S19 |
11 | BAA08g03260 | A08 | 2269369 | G | A | upstream_gene_variant | MODIFIER | c.-310G>A| |
S62 |
12 | BAA08g03260 | A08 | 2269533 | G | A | upstream_gene_variant | MODIFIER | c.-146G>A| |
S115 |
13 | BAA08g03260 | A08 | 2269827 | C | T | missense_variant | MODERATE | c.149C>T|p.Ala50Val |
S114 |
14 | BAA08g03260 | A08 | 2269856 | G | A | missense_variant&splice_region_variant | MODERATE | c.178G>A|p.Asp60Asn |
S282 |
15 | BAA08g03260 | A08 | 2270307 | C | T | missense_variant | MODERATE | c.334C>T|p.Leu112Phe |
S291 |
16 | BAA08g03260 | A08 | 2270378 | G | A | missense_variant | MODERATE | c.405G>A|p.Met135Ile |
S282 |
17 | BAA08g03260 | A08 | 2270591 | C | T | synonymous_variant | LOW | c.519C>T|p.Asn173Asn |
S46 |
18 | BAA08g03260 | A08 | 2275465 | C | T | downstream_gene_variant | MODIFIER | c.*4323C>T| |
S192 |