Users can query the SNP information according to the gene ID.


Gene ID

Results: 1 - 14 of 14 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
1 BAA09g33550 A09 42096172 C T upstream_gene_variant MODIFIER c.-4874C>T| S36
2 BAA09g33550 A09 42096871 C T upstream_gene_variant MODIFIER c.-4175C>T| S168
3 BAA09g33550 A09 42097244 C T upstream_gene_variant MODIFIER c.-3802C>T| S241
4 BAA09g33550 A09 42097248 C T upstream_gene_variant MODIFIER c.-3798C>T| S97
5 BAA09g33550 A09 42097704 C T upstream_gene_variant MODIFIER c.-3342C>T| S295
6 BAA09g33550 A09 42098239 G A upstream_gene_variant MODIFIER c.-2807G>A| S156
7 BAA09g33550 A09 42098366 C T upstream_gene_variant MODIFIER c.-2680C>T| S302
8 BAA09g33550 A09 42098885 G T upstream_gene_variant MODIFIER c.-2161G>T| S15
S3
9 BAA09g33550 A09 42099612 G A upstream_gene_variant MODIFIER c.-1434G>A| S81
S85
10 BAA09g33550 A09 42100449 G A upstream_gene_variant MODIFIER c.-597G>A| S76
11 BAA09g33550 A09 42100568 C T upstream_gene_variant MODIFIER c.-478C>T| S36
12 BAA09g33550 A09 42101060 G A synonymous_variant LOW c.15G>A|p.Glu5Glu S88
13 BAA09g33550 A09 42101408 C T synonymous_variant LOW c.363C>T|p.Phe121Phe S297
14 BAA09g33550 A09 42101718 G A splice_region_variant&intron_variant LOW c.478-5G>A| S218