Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g16990 | A08 | 13898761 | G | A | upstream_gene_variant | MODIFIER | c.-4422G>A| |
S298 |
2 | BAA08g16990 | A08 | 13898806 | C | T | upstream_gene_variant | MODIFIER | c.-4377C>T| |
S79 S84 |
3 | BAA08g16990 | A08 | 13899590 | C | T | upstream_gene_variant | MODIFIER | c.-3593C>T| |
|
4 | BAA08g16990 | A08 | 13900462 | G | A | upstream_gene_variant | MODIFIER | c.-2721G>A| |
S92 |
5 | BAA08g16990 | A08 | 13900640 | G | T | upstream_gene_variant | MODIFIER | c.-2543G>T| |
S201 |
6 | BAA08g16990 | A08 | 13900943 | G | A | upstream_gene_variant | MODIFIER | c.-2240G>A| |
S41 |
7 | BAA08g16990 | A08 | 13901259 | C | T | upstream_gene_variant | MODIFIER | c.-1924C>T| |
S276 |
8 | BAA08g16990 | A08 | 13903568 | G | A | missense_variant | MODERATE | c.386G>A|p.Ser129Asn |
S269 |
9 | BAA08g16990 | A08 | 13904251 | C | T | splice_region_variant&intron_variant | LOW | c.430-3C>T| |
S277 |
10 | BAA08g16990 | A08 | 13904296 | C | T | downstream_gene_variant | MODIFIER | c.*40C>T| |
S168 |
11 | BAA08g16990 | A08 | 13906142 | C | T | downstream_gene_variant | MODIFIER | c.*1886C>T| |
S250 |
12 | BAA08g16990 | A08 | 13907390 | C | T | downstream_gene_variant | MODIFIER | c.*3134C>T| |
S186 |
13 | BAA08g16990 | A08 | 13908450 | G | A | downstream_gene_variant | MODIFIER | c.*4194G>A| |
S182 |
14 | BAA08g16990 | A08 | 13908745 | G | A | downstream_gene_variant | MODIFIER | c.*4489G>A| |
S203 |
15 | BAA08g16990 | A08 | 13909076 | C | T | downstream_gene_variant | MODIFIER | c.*4820C>T| |
S201 |
16 | BAA08g16990 | A08 | 13909090 | C | T | downstream_gene_variant | MODIFIER | c.*4834C>T| |
S88 |