73 results
Allele/Variant Genes: Wdr55 (Mmu)

Wdr55tm1Matn

(Mus musculus)
Allele/Variant
Source: MGI:3580272
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Wdr55tm1(KOMP)Vlcg

(Mus musculus)
Allele/Variant
Source: MGI:4452983
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

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: rs581308290
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896605A>T

Allele/Variant
Source: rs244711889
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896675A>C

Allele/Variant
Source: rs257873047
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896682T>C

Allele/Variant
Source: rs219855503
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896639A>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: rs245792236
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895456G>C

Allele/Variant
Source: rs31793364
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36893345C>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: rs1134214543
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896244G>A

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: rs31792528
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896564G>A

Allele/Variant
Source: rs216786568
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36893337C>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: rs232117941
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896040T>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: 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: rs31792531
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895789A>G

Allele/Variant
Source: rs31792530
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896030T>C

Allele/Variant
Source: rs583563328
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896587T>A

Allele/Variant
Source: rs586932298
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896604C>T

Allele/Variant
Source: rs240103461
Genes: Dnd1 (Mmu), Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896777A>G

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: 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: 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: rs31792527
Genes: Dnd1 (Mmu), Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896828G>T

Allele/Variant
Source: rs1132094653
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896640A>G

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: rs265456576
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896198G>T