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


Gene ID

Results: 1 - 16 of 16 records


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