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
168501 BAA02g13780 A02 6433444 G A upstream_gene_variant MODIFIER c.-39C>T| S25
168502 BAA02g13790 A02 6434403 C T missense_variant MODERATE c.1504G>A|p.Glu502Lys S135
168503 BAA02g13780 A02 6436957 G A upstream_gene_variant MODIFIER c.-3552C>T| S139
168504 BAA02g13780 A02 6437035 A G upstream_gene_variant MODIFIER c.-3630T>C| S208
S219
168505 BAA02g13780 A02 6437431 C T upstream_gene_variant MODIFIER c.-4026G>A| S104
168506 BAA02g13790 A02 6439926 G A upstream_gene_variant MODIFIER c.-3753C>T| S23
168507 BAA02g13800 A02 6443376 C T downstream_gene_variant MODIFIER c.*1636G>A| S108
168508 BAA02g13800 A02 6443653 G A downstream_gene_variant MODIFIER c.*1359C>T| S296
168509 BAA02g13800 A02 6445362 C T missense_variant MODERATE c.1384G>A|p.Glu462Lys S1
S90
168510 BAA02g13800 A02 6445530 G A missense_variant MODERATE c.1216C>T|p.Leu406Phe S236
168511 BAA02g13800 A02 6447711 C T missense_variant MODERATE c.409G>A|p.Glu137Lys S75
S81
168512 BAA02g13800 A02 6447726 C T missense_variant MODERATE c.394G>A|p.Glu132Lys S270
168513 BAA02g13800 A02 6447811 C T synonymous_variant LOW c.309G>A|p.Lys103Lys S18
168514 BAA02g13800 A02 6448786 G A upstream_gene_variant MODIFIER c.-667C>T| S80
168515 BAA02g13800 A02 6449561 G A upstream_gene_variant MODIFIER c.-1442C>T| S45
168516 BAA02g13800 A02 6449828 C T upstream_gene_variant MODIFIER c.-1709G>A| S219
168517 BAA02g13800 A02 6450026 G A upstream_gene_variant MODIFIER c.-1907C>T| S37
168518 BAA02g13800 A02 6450287 C T upstream_gene_variant MODIFIER c.-2168G>A| S131
168519 BAA02g13800 A02 6450331 G A upstream_gene_variant MODIFIER c.-2212C>T| S92
168520 BAA02g13800 A02 6451174 G A upstream_gene_variant MODIFIER c.-3055C>T| S192
168521 BAA02g13800 A02 6452198 G A upstream_gene_variant MODIFIER c.-4079C>T| S79
S91
168522 BAA02g13810 A02 6452578 C T missense_variant MODERATE c.1003G>A|p.Ala335Thr S40
S49
168523 BAA02g13810 A02 6453389 G A missense_variant MODERATE c.418C>T|p.Pro140Ser S174
168524 BAA02g13810 A02 6453755 G A missense_variant MODERATE c.137C>T|p.Pro46Leu S11
168525 BAA02g13810 A02 6453992 G A intron_variant MODIFIER c.65-165C>T| S295