43 results
Allele/Variant Genes: Wdr55 (Mmu) Molecular Consequence: non coding transcript variant
Allele/Variant
Source: rs31792533
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894569G>A

Allele/Variant
Source: rs245820426
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894608C>T

Allele/Variant
Source: rs212240740
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894611G>A

Allele/Variant
Source: rs585519379
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894808G>C

Allele/Variant
Source: rs248308583
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895358C>T

Allele/Variant
Source: rs226195240
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895387T>G

Allele/Variant
Source: rs258150599
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895878A>G

Allele/Variant
Source: rs245219040
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36893890C>T

Allele/Variant
Source: rs245337306
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894307A>T

Allele/Variant
Source: rs30014790
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894654C>T

Allele/Variant
Source: rs238054915
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894798C>G

Allele/Variant
Source: rs227117165
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36893802C>T

Allele/Variant
Source: rs264165223
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894363G>T

Allele/Variant
Source: rs579466082
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895840A>G

Allele/Variant
Source: rs265989767
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895157C>T

Allele/Variant
Source: rs234146881
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895161C>T

Allele/Variant
Source: rs253680550
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894296G>T

Allele/Variant
Source: rs215952200
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894557A>G

Allele/Variant
Source: rs263677395
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894615G>A

Allele/Variant
Source: rs259460914
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894686A>G

Allele/Variant
Source: rs583938477
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894802G>C

Allele/Variant
Source: rs218900938
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895629G>C

Allele/Variant
Source: rs247831354
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896118T>C

Allele/Variant
Source: rs218398011
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896128C>T

Allele/Variant
Source: rs212277723
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36893593A>C

Allele/Variant
Source: rs252239743
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36893565A>G

Allele/Variant
Source: rs580461976
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894278G>A

Allele/Variant
Source: rs235673153
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894374C>T

Allele/Variant
Source: rs252721033
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894472C>A

Allele/Variant
Source: rs230462784
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36893615T>C

Allele/Variant
Source: rs260188764
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36893670A>G

Allele/Variant
Source: rs263141807
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894117G>A

Allele/Variant
Source: rs586064591
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894148G>C

Allele/Variant
Source: rs260270230
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895369G>A

Allele/Variant
Source: rs254117518
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895627A>G

Allele/Variant
Source: rs219374103
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894796G>A

Allele/Variant
Source: rs219115912
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894129G>A

Allele/Variant
Source: rs238089834
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894240C>T

Allele/Variant
Source: rs224155074
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894298T>G

Allele/Variant
Source: rs230915269
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894614G>A

Allele/Variant
Source: rs239907643
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894659T>C

Allele/Variant
Source: rs247905013
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36894980G>A

Allele/Variant
Source: rs31792532
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895137A>G