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
160451 BAA02g07660 A02 3291484 C T upstream_gene_variant MODIFIER c.-877G>A| S180
160452 BAA02g07660 A02 3291557 G A upstream_gene_variant MODIFIER c.-950C>T| S202
160453 BAA02g07660 A02 3292518 G A upstream_gene_variant MODIFIER c.-1911C>T| S84
S93
160454 BAA02g07670 A02 3293098 G A synonymous_variant LOW c.78G>A|p.Gly26Gly S176
160455 BAA02g07660 A02 3293438 G A upstream_gene_variant MODIFIER c.-2831C>T| S303
160456 BAA02g07670 A02 3294292 G A missense_variant MODERATE c.922G>A|p.Glu308Lys S128
160457 BAA02g07680 A02 3295477 G A synonymous_variant LOW c.1716C>T|p.Ser572Ser S202
160458 BAA02g07680 A02 3295784 C T missense_variant MODERATE c.1409G>A|p.Arg470Lys S298
160459 BAA02g07680 A02 3296160 G A missense_variant MODERATE c.1033C>T|p.Pro345Ser S107
160460 BAA02g07680 A02 3296323 C T synonymous_variant LOW c.870G>A|p.Glu290Glu S38
160461 BAA02g07690 A02 3297592 G A missense_variant MODERATE c.22G>A|p.Ala8Thr S157
160462 BAA02g07690 A02 3297996 G A synonymous_variant LOW c.426G>A|p.Ser142Ser S264
160463 BAA02g07690 A02 3298197 C T synonymous_variant LOW c.627C>T|p.Leu209Leu S71
160464 BAA02g07690 A02 3298666 G A missense_variant MODERATE c.1096G>A|p.Gly366Arg S92
160465 BAA02g07690 A02 3298691 G A missense_variant MODERATE c.1121G>A|p.Gly374Glu S232
160466 BAA02g07690 A02 3298867 C T missense_variant MODERATE c.1297C>T|p.Pro433Ser S295
160467 BAA02g07690 A02 3300798 G A synonymous_variant LOW c.3228G>A|p.Arg1076Arg S136
160468 BAA02g07680 A02 3302528 G A upstream_gene_variant MODIFIER c.-4969C>T| S113
160469 BAA02g07700 A02 3304253 G A missense_variant MODERATE c.485C>T|p.Ala162Val S122
160470 BAA02g07700 A02 3305783 C T upstream_gene_variant MODIFIER c.-1046G>A| S202
160471 BAA02g07710 A02 3306166 C T missense_variant MODERATE c.584G>A|p.Gly195Glu S16
160472 BAA02g07700 A02 3307149 C T upstream_gene_variant MODIFIER c.-2412G>A| S252
160473 BAA02g07710 A02 3307392 G C missense_variant MODERATE c.56C>G|p.Thr19Arg S291
160474 BAA02g07700 A02 3308272 C T upstream_gene_variant MODIFIER c.-3535G>A| S295
160475 BAA02g07700 A02 3309384 G A upstream_gene_variant MODIFIER c.-4647C>T| S239