Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26820 | A02 | 15024468 | G | A | upstream_gene_variant | MODIFIER | c.-4383G>A| |
S169 |
2 | BAA02g26820 | A02 | 15024950 | C | T | upstream_gene_variant | MODIFIER | c.-3901C>T| |
S124 S126 S127 S128 S131 S190 S223 S255 S284 S57 S59 |
3 | BAA02g26820 | A02 | 15024965 | C | T | upstream_gene_variant | MODIFIER | c.-3886C>T| |
S130 |
4 | BAA02g26820 | A02 | 15025945 | G | A | upstream_gene_variant | MODIFIER | c.-2906G>A| |
S71 |
5 | BAA02g26820 | A02 | 15026480 | G | A | upstream_gene_variant | MODIFIER | c.-2371G>A| |
S281 |
6 | BAA02g26820 | A02 | 15026783 | C | T | upstream_gene_variant | MODIFIER | c.-2068C>T| |
S208 S93 |
7 | BAA02g26820 | A02 | 15027990 | C | T | upstream_gene_variant | MODIFIER | c.-861C>T| |
S293 |
8 | BAA02g26820 | A02 | 15028546 | C | T | upstream_gene_variant | MODIFIER | c.-305C>T| |
S226 |
9 | BAA02g26820 | A02 | 15028809 | C | T | upstream_gene_variant | MODIFIER | c.-42C>T| |
S112 |
10 | BAA02g26820 | A02 | 15028983 | C | T | missense_variant | MODERATE | c.133C>T|p.Pro45Ser |
S270 |
11 | BAA02g26820 | A02 | 15028991 | G | A | synonymous_variant | LOW | c.141G>A|p.Leu47Leu |
S161 |
12 | BAA02g26820 | A02 | 15029335 | C | T | synonymous_variant | LOW | c.396C>T|p.Ile132Ile |
S138 |
13 | BAA02g26820 | A02 | 15030307 | C | T | splice_region_variant&intron_variant | LOW | c.739-3C>T| |
S144 |
14 | BAA02g26820 | A02 | 15033574 | C | T | downstream_gene_variant | MODIFIER | c.*2716C>T| |
S2 |
15 | BAA02g26820 | A02 | 15033923 | G | A | downstream_gene_variant | MODIFIER | c.*3065G>A| |
S44 |
16 | BAA02g26820 | A02 | 15034221 | G | A | downstream_gene_variant | MODIFIER | c.*3363G>A| |
S92 |