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
138651 BAA10g24110 A10 19992537 G A upstream_gene_variant MODIFIER c.-2055C>T| S139
138652 BAA10g24110 A10 19993239 C T upstream_gene_variant MODIFIER c.-2757G>A| S292
138653 BAA10g24110 A10 19993391 G A upstream_gene_variant MODIFIER c.-2909C>T| S62
138654 BAA10g24110 A10 19994567 G A upstream_gene_variant MODIFIER c.-4085C>T| S77
S82
138655 BAA10g24110 A10 19994578 C T upstream_gene_variant MODIFIER c.-4096G>A| S84
138656 BAA10g24130 A10 19995901 G A missense_variant MODERATE c.310C>T|p.Leu104Phe S172
S217
138657 BAA10g24130 A10 19996139 G A synonymous_variant LOW c.72C>T|p.Leu24Leu S69
138658 BAA10g24120 A10 19996421 G A upstream_gene_variant MODIFIER c.-4590C>T| S55
138659 BAA10g24120 A10 19996737 C T upstream_gene_variant MODIFIER c.-4906G>A| S210
138660 BAA10g24130 A10 19997458 G A upstream_gene_variant MODIFIER c.-1248C>T| S9
138661 BAA10g24130 A10 19998045 C T upstream_gene_variant MODIFIER c.-1835G>A| S152
138662 BAA10g24130 A10 19998549 C T upstream_gene_variant MODIFIER c.-2339G>A| S274
138663 BAA10g24130 A10 19998690 G A upstream_gene_variant MODIFIER c.-2480C>T| S293
138664 BAA10g24130 A10 19999129 C G upstream_gene_variant MODIFIER c.-2919G>C| S105
S107
S125
S127
S129
S203
S237
S250
S298
S38
S48
S66
138665 BAA10g24140 A10 20000472 G A missense_variant MODERATE c.355G>A|p.Asp119Asn S236
138666 BAA10g24130 A10 20001052 G A upstream_gene_variant MODIFIER c.-4842C>T| S66
138667 BAA10g24150 A10 20001560 G A upstream_gene_variant MODIFIER c.-1729G>A| S195
138668 BAA10g24150 A10 20003308 C T missense_variant MODERATE c.20C>T|p.Ala7Val S68
138669 BAA10g24150 A10 20004150 G A stop_gained HIGH c.780G>A|p.Trp260* S241
138670 BAA10g24150 A10 20004329 C T missense_variant MODERATE c.959C>T|p.Ala320Val S292
138671 BAA10g24160 A10 20005115 C T synonymous_variant LOW c.792G>A|p.Glu264Glu S12
138672 BAA10g24160 A10 20006047 C T missense_variant MODERATE c.349G>A|p.Asp117Asn S269
138673 BAA10g24160 A10 20006786 C T upstream_gene_variant MODIFIER c.-37G>A| S92
138674 BAA10g24160 A10 20006820 C T upstream_gene_variant MODIFIER c.-71G>A| S205
138675 BAA10g24160 A10 20007658 C T upstream_gene_variant MODIFIER c.-909G>A| S42