30 results
Allele/Variant Genes: Wdr55 (Mmu) Molecular Consequence: non coding transcript variant

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: 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: 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: 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: 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: 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: 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: 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: 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: 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: 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

Allele/Variant
Source: rs260232940
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)18:36896579A>G

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: rs212158083
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895475A>G

Allele/Variant
Source: rs229396251
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895543C>T

Allele/Variant
Source: rs232079433
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)18:36896654T>G

Allele/Variant
Source: rs1134902469
Genes: Dnd1 (Mmu), Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896791C>G

Allele/Variant
Source: rs218429326
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36895066A>G

Allele/Variant
Source: rs13468285
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896204C>T

Allele/Variant
Source: rs260699394
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896302G>T

Allele/Variant
Source: rs31792529
Genes: Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896422A>C

Allele/Variant
Source: rs227465828
Genes: Dnd1 (Mmu), Wdr55 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)18:36896794G>A