Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22110 | A01 | 11024840 | G | A | upstream_gene_variant | MODIFIER | c.-4667G>A| |
S161 |
2 | BAA01g22110 | A01 | 11025481 | C | T | upstream_gene_variant | MODIFIER | c.-4026C>T| |
S198 |
3 | BAA01g22110 | A01 | 11025846 | C | T | upstream_gene_variant | MODIFIER | c.-3661C>T| |
S282 |
4 | BAA01g22110 | A01 | 11026307 | C | A | upstream_gene_variant | MODIFIER | c.-3200C>A| |
S44 |
5 | BAA01g22110 | A01 | 11027294 | C | T | upstream_gene_variant | MODIFIER | c.-2213C>T| |
S63 |
6 | BAA01g22110 | A01 | 11027369 | C | T | upstream_gene_variant | MODIFIER | c.-2138C>T| |
S19 |
7 | BAA01g22110 | A01 | 11027602 | C | T | upstream_gene_variant | MODIFIER | c.-1905C>T| |
S233 |
8 | BAA01g22110 | A01 | 11029844 | G | A | intron_variant | MODIFIER | c.166-90G>A| |
S287 |
9 | BAA01g22110 | A01 | 11029899 | G | A | intron_variant | MODIFIER | c.166-35G>A| |
S187 |
10 | BAA01g22110 | A01 | 11030982 | G | A | synonymous_variant | LOW | c.729G>A|p.Lys243Lys |
S123 |
11 | BAA01g22110 | A01 | 11031691 | C | T | intron_variant | MODIFIER | c.1047+37C>T| |
S182 |
12 | BAA01g22110 | A01 | 11031699 | C | T | intron_variant | MODIFIER | c.1048-37C>T| |
S67 |
13 | BAA01g22110 | A01 | 11032311 | G | A | missense_variant | MODERATE | c.1340G>A|p.Arg447Lys |
S96 |
14 | BAA01g22110 | A01 | 11032331 | C | T | missense_variant | MODERATE | c.1360C>T|p.Leu454Phe |
S211 S227 |
15 | BAA01g22110 | A01 | 11032675 | C | T | intron_variant | MODIFIER | c.1604+19C>T| |
S183 |
16 | BAA01g22110 | A01 | 11034764 | C | T | downstream_gene_variant | MODIFIER | c.*893C>T| |
S289 S290 |