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
161051 BAA02g08200 A02 3516906 C T synonymous_variant LOW c.144G>A|p.Glu48Glu S179
161052 BAA02g08190 A02 3517405 C T upstream_gene_variant MODIFIER c.-3757G>A| S81
161053 BAA02g08190 A02 3517815 G A upstream_gene_variant MODIFIER c.-4167C>T| S144
161054 BAA02g08200 A02 3518665 G A upstream_gene_variant MODIFIER c.-1616C>T| S105
S106
161055 BAA02g08200 A02 3518797 G A upstream_gene_variant MODIFIER c.-1748C>T| S164
161056 BAA02g08200 A02 3519293 G A upstream_gene_variant MODIFIER c.-2244C>T| S283
161057 BAA02g08210 A02 3520307 G A missense_variant MODERATE c.137G>A|p.Arg46Lys S57
161058 BAA02g08200 A02 3521878 G A upstream_gene_variant MODIFIER c.-4829C>T| S200
S261
S303
161059 BAA02g08220 A02 3525576 C T missense_variant MODERATE c.241C>T|p.Pro81Ser S129
161060 BAA02g08220 A02 3526030 C T missense_variant MODERATE c.695C>T|p.Ser232Phe S224
161061 BAA02g08220 A02 3526089 G A missense_variant MODERATE c.754G>A|p.Asp252Asn S144
161062 BAA02g08220 A02 3526199 G A synonymous_variant LOW c.864G>A|p.Arg288Arg S228
161063 BAA02g08220 A02 3526487 C T synonymous_variant LOW c.1152C>T|p.Phe384Phe S276
161064 BAA02g08230 A02 3526961 C T missense_variant MODERATE c.1151G>A|p.Gly384Glu S230
161065 BAA02g08230 A02 3530373 C T upstream_gene_variant MODIFIER c.-2262G>A| S18
161066 BAA02g08240 A02 3530940 G A missense_variant MODERATE c.1313C>T|p.Ser438Phe S205
161067 BAA02g08240 A02 3531328 C T missense_variant MODERATE c.1016G>A|p.Gly339Glu S262
161068 BAA02g08240 A02 3532528 G A splice_region_variant&intron_variant LOW c.241-6C>T| S119
161069 BAA02g08230 A02 3532830 C T upstream_gene_variant MODIFIER c.-4719G>A| S38
161070 BAA02g08230 A02 3533026 G A upstream_gene_variant MODIFIER c.-4915C>T| S244
161071 BAA02g08240 A02 3533409 G A upstream_gene_variant MODIFIER c.-586C>T| S209
161072 BAA02g08240 A02 3534194 G A upstream_gene_variant MODIFIER c.-1371C>T| S92
161073 BAA02g08240 A02 3534277 G A upstream_gene_variant MODIFIER c.-1454C>T| S287
161074 BAA02g08250 A02 3535134 G A splice_region_variant&intron_variant LOW c.602+5G>A| S209
161075 BAA02g08250 A02 3535750 C A missense_variant MODERATE c.1013C>A|p.Pro338Gln S177