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
151351 BAA02g00120 A02 93167 G A missense_variant MODERATE c.256G>A|p.Val86Ile S162
151352 BAA02g00100 A02 93423 C T upstream_gene_variant MODIFIER c.-4418G>A| S200
151353 BAA02g00100 A02 93717 G A upstream_gene_variant MODIFIER c.-4712C>T| S282
151354 BAA02g00110 A02 94466 G A upstream_gene_variant MODIFIER c.-2605C>T| S121
151355 BAA02g00110 A02 96565 C T upstream_gene_variant MODIFIER c.-4704G>A| S245
151356 BAA02g00130 A02 99475 C T upstream_gene_variant MODIFIER c.-2680G>A| S115
151357 BAA02g00140 A02 102582 G A downstream_gene_variant MODIFIER c.*4576C>T| S232
151358 BAA02g00140 A02 102803 G A downstream_gene_variant MODIFIER c.*4355C>T| S53
151359 BAA02g00140 A02 107045 C T downstream_gene_variant MODIFIER c.*113G>A| S65
151360 BAA02g00140 A02 107676 G A upstream_gene_variant MODIFIER c.-36C>T| S47
151361 BAA02g00140 A02 108892 C T upstream_gene_variant MODIFIER c.-1252G>A| S69
151362 BAA02g00140 A02 108927 G A upstream_gene_variant MODIFIER c.-1287C>T| S282
151363 BAA02g00140 A02 110093 G A upstream_gene_variant MODIFIER c.-2453C>T| S266
151364 BAA02g00140 A02 110820 G A upstream_gene_variant MODIFIER c.-3180C>T| S11
151365 BAA02g00140 A02 111036 C T upstream_gene_variant MODIFIER c.-3396G>A| S71
151366 BAA02g00150 A02 112945 G A upstream_gene_variant MODIFIER c.-2467G>A| S33
151367 BAA02g00150 A02 113484 C T upstream_gene_variant MODIFIER c.-1928C>T| S283
151368 BAA02g00150 A02 114534 G A upstream_gene_variant MODIFIER c.-878G>A| S208
S219
151369 BAA02g00150 A02 114616 G A upstream_gene_variant MODIFIER c.-796G>A| S302
151370 BAA02g00150 A02 115157 C T upstream_gene_variant MODIFIER c.-255C>T| S249
151371 BAA02g00150 A02 115352 C T upstream_gene_variant MODIFIER c.-60C>T| S255
151372 BAA02g00150 A02 115460 G A missense_variant MODERATE c.49G>A|p.Val17Ile S12
151373 BAA02g00150 A02 116307 G A missense_variant MODERATE c.896G>A|p.Gly299Asp S237
151374 BAA02g00150 A02 116609 G A missense_variant MODERATE c.1198G>A|p.Gly400Arg S148
S30
S31
151375 BAA02g00150 A02 116699 C T synonymous_variant LOW c.1288C>T|p.Leu430Leu S181