Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44470 | A02 | 36623421 | C | T | upstream_gene_variant | MODIFIER | c.-4920C>T| |
S123 |
2 | BAA02g44470 | A02 | 36624809 | C | T | upstream_gene_variant | MODIFIER | c.-3532C>T| |
S263 |
3 | BAA02g44470 | A02 | 36625209 | G | A | upstream_gene_variant | MODIFIER | c.-3132G>A| |
S45 |
4 | BAA02g44470 | A02 | 36625510 | G | A | upstream_gene_variant | MODIFIER | c.-2831G>A| |
S72 S78 |
5 | BAA02g44470 | A02 | 36626097 | C | T | upstream_gene_variant | MODIFIER | c.-2244C>T| |
S173 |
6 | BAA02g44470 | A02 | 36626232 | G | A | upstream_gene_variant | MODIFIER | c.-2109G>A| |
S79 S91 |
7 | BAA02g44470 | A02 | 36627231 | C | T | upstream_gene_variant | MODIFIER | c.-1110C>T| |
S206 S26 |
8 | BAA02g44470 | A02 | 36628978 | G | A | missense_variant | MODERATE | c.379G>A|p.Glu127Lys |
S28 |
9 | BAA02g44470 | A02 | 36629312 | C | T | intron_variant | MODIFIER | c.500+213C>T| |
S59 |
10 | BAA02g44470 | A02 | 36629493 | C | T | intron_variant | MODIFIER | c.501-348C>T| |
S129 |
11 | BAA02g44470 | A02 | 36630266 | G | A | missense_variant | MODERATE | c.788G>A|p.Ser263Asn |
S89 |
12 | BAA02g44470 | A02 | 36630372 | C | T | splice_region_variant&intron_variant | LOW | c.888+6C>T| |
S109 |
13 | BAA02g44470 | A02 | 36630958 | C | T | stop_gained | HIGH | c.1210C>T|p.Gln404* |
S201 |