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
179051 BAA02g19720 A02 10266069 G A missense_variant MODERATE c.334C>T|p.Arg112Cys S291
179052 BAA02g19720 A02 10266209 C T missense_variant MODERATE c.194G>A|p.Arg65Lys S299
179053 BAA02g19700 A02 10266321 C T upstream_gene_variant MODIFIER c.-4525G>A| S58
179054 BAA02g19720 A02 10267072 G A upstream_gene_variant MODIFIER c.-593C>T| S35
179055 BAA02g19720 A02 10267322 C T upstream_gene_variant MODIFIER c.-843G>A| S305
179056 BAA02g19720 A02 10267757 G A upstream_gene_variant MODIFIER c.-1278C>T| S237
179057 BAA02g19720 A02 10268664 G A upstream_gene_variant MODIFIER c.-2185C>T| S34
179058 BAA02g19720 A02 10269039 G A upstream_gene_variant MODIFIER c.-2560C>T| S59
179059 BAA02g19720 A02 10269611 G A upstream_gene_variant MODIFIER c.-3132C>T| S19
179060 BAA02g19720 A02 10270460 G A upstream_gene_variant MODIFIER c.-3981C>T| S225
179061 BAA02g19720 A02 10270629 T C upstream_gene_variant MODIFIER c.-4150A>G| S182
179062 BAA02g19730 A02 10272782 C T downstream_gene_variant MODIFIER c.*647G>A| S25
179063 BAA02g19730 A02 10272901 G A downstream_gene_variant MODIFIER c.*528C>T| S291
179064 BAA02g19730 A02 10273601 C T missense_variant MODERATE c.80G>A|p.Gly27Glu S118
179065 BAA02g19730 A02 10273708 G A upstream_gene_variant MODIFIER c.-28C>T| S95
179066 BAA02g19730 A02 10273875 C T upstream_gene_variant MODIFIER c.-195G>A| S115
179067 BAA02g19730 A02 10274101 G A upstream_gene_variant MODIFIER c.-421C>T| S35
179068 BAA02g19730 A02 10274313 G A upstream_gene_variant MODIFIER c.-633C>T| S148
S191
S30
S31
179069 BAA02g19730 A02 10276117 C T upstream_gene_variant MODIFIER c.-2437G>A| S292
179070 BAA02g19730 A02 10276603 C T upstream_gene_variant MODIFIER c.-2923G>A| S112
179071 BAA02g19730 A02 10277030 G A upstream_gene_variant MODIFIER c.-3350C>T| S251
179072 BAA02g19730 A02 10277099 G A upstream_gene_variant MODIFIER c.-3419C>T| S45
179073 BAA02g19730 A02 10277750 G C upstream_gene_variant MODIFIER c.-4070C>G| S117
S174
S228
S236
S40
S5
179074 BAA02g19730 A02 10278478 C T upstream_gene_variant MODIFIER c.-4798G>A| S118
179075 BAA02g19740 A02 10279399 C T intron_variant MODIFIER c.3190-3885G>A| S267