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


Gene ID

Results: 1 - 489298 of 489298 records


Num GeneID Chromosome Position Ref.allele Alt.allele Mutant type Impacts Amino acid change SampleID
54051 BAA01g29680 A01 18755818 C T upstream_gene_variant MODIFIER c.-478G>A| S150
54052 BAA01g29680 A01 18755872 C T upstream_gene_variant MODIFIER c.-532G>A| S46
54053 BAA01g29680 A01 18756030 C A upstream_gene_variant MODIFIER c.-690G>T| S33
54054 BAA01g29680 A01 18756316 C T upstream_gene_variant MODIFIER c.-976G>A| S276
54055 BAA01g29680 A01 18756734 G A upstream_gene_variant MODIFIER c.-1394C>T| S138
54056 BAA01g29680 A01 18757309 G A upstream_gene_variant MODIFIER c.-1969C>T| S308
54057 BAA01g29680 A01 18759886 G A upstream_gene_variant MODIFIER c.-4546C>T| S25
54058 BAA01g29680 A01 18760007 C T upstream_gene_variant MODIFIER c.-4667G>A| S66
54059 BAA01g29690 A01 18760628 C T upstream_gene_variant MODIFIER c.-3978C>T| S115
54060 BAA01g29690 A01 18761742 G A upstream_gene_variant MODIFIER c.-2864G>A| S140
S168
S219
S279
S301
54061 BAA01g29690 A01 18764470 C T upstream_gene_variant MODIFIER c.-136C>T| S167
54062 BAA01g29690 A01 18764549 G A upstream_gene_variant MODIFIER c.-57G>A| S13
S140
S168
S219
S279
54063 BAA01g29690 A01 18764827 G A intron_variant MODIFIER c.54-37G>A| S257
54064 BAA01g29690 A01 18765504 C T intron_variant MODIFIER c.487-33C>T| S155
S211
54065 BAA01g29690 A01 18765618 G A missense_variant MODERATE c.568G>A|p.Gly190Arg S15
S3
54066 BAA01g29690 A01 18765885 G A splice_acceptor_variant&intron_variant HIGH c.628-1G>A| S55
54067 BAA01g29690 A01 18766386 G A synonymous_variant LOW c.921G>A|p.Lys307Lys S174
S27
54068 BAA01g29690 A01 18768846 C T stop_gained HIGH c.2707C>T|p.Gln903* S42
54069 BAA01g29690 A01 18768909 C T intron_variant MODIFIER c.2724+46C>T| S143
54070 BAA01g29690 A01 18769204 C T stop_gained HIGH c.2887C>T|p.Gln963* S184
54071 BAA01g29690 A01 18769237 G A missense_variant MODERATE c.2920G>A|p.Gly974Arg S199
54072 BAA01g29690 A01 18769549 C T synonymous_variant LOW c.3141C>T|p.Cys1047Cys S198
54073 BAA01g29690 A01 18770501 C T downstream_gene_variant MODIFIER c.*675C>T| S279
54074 BAA01g29690 A01 18770777 C T downstream_gene_variant MODIFIER c.*951C>T| S242
54075 BAA01g29690 A01 18771766 G A downstream_gene_variant MODIFIER c.*1940G>A| S257