1,822 results
Allele/Variant Genes: Wdr59 (Mmu)

Wdr59tm1a(EUCOMM)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:4461692
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Wdr59tm1b(EUCOMM)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:5548803
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs586885174
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112186437C>T

Allele/Variant
Source: rs584334383
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112186796T>C

Allele/Variant
Source: rs240594454
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112186973A>G

Allele/Variant
Source: rs256286530
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112184963C>T

Allele/Variant
Source: rs585578136
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112185133C>A

Allele/Variant
Source: rs237734066
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112175583C>G

Allele/Variant
Source: rs31307582
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112175591C>T

Allele/Variant
Source: rs244534677
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112177877T>C

Allele/Variant
Source: rs248091728
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112179680C>A

Allele/Variant
Source: rs251688698
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112177029A>G

Allele/Variant
Source: rs250482711
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112176127C>T

Allele/Variant
Source: rs587426587
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112176306C>T

Allele/Variant
Source: rs220266359
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112181788T>C

Allele/Variant
Source: rs245800174
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112180904G>T

Allele/Variant
Source: rs245904346
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112182261T>C

Allele/Variant
Source: rs236287365
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112183008C>T

Allele/Variant
Source: rs262177212
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112182737C>T

Allele/Variant
Source: rs228172299
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112183381G>A

Allele/Variant
Source: rs262096790
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112183937C>T

Allele/Variant
Source: rs220453326
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112183958A>G

Allele/Variant
Source: rs258752934
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112209183T>A

Allele/Variant
Source: rs263743854
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112195400C>T

Allele/Variant
Source: rs586503649
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112195908C>A

Allele/Variant
Source: rs238896004
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112196124G>A

Allele/Variant
Source: rs233019317
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112209496T>G

Allele/Variant
Source: rs264713373
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112205266C>G

Allele/Variant
Source: rs249916559
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112197044A>G

Allele/Variant
Source: rs238642335
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112197504G>A

Allele/Variant
Source: rs1134180753
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112197696C>A

Allele/Variant
Source: rs31307749
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112226996A>G

Allele/Variant
Source: rs578517107
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112177411A>C

Allele/Variant
Source: rs241907404
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112206367G>A

Allele/Variant
Source: rs255535295
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112207511G>A

Allele/Variant
Source: rs226563722
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112198206A>T

Allele/Variant
Source: rs226420963
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112207822T>C

Allele/Variant
Source: rs585016370
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112189681T>C

Allele/Variant
Source: rs246309097
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112189764A>T

Allele/Variant
Source: rs262645369
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112192628C>T

Allele/Variant
Source: rs31311536
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112192745C>T

Allele/Variant
Source: rs222476039
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112194387T>C

Allele/Variant
Source: rs230105985
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112190305T>G

Allele/Variant
Source: rs212764242
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112207859T>C

Allele/Variant
Source: rs244218118
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112189563G>A

Allele/Variant
Source: rs108109916
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112192313G>A

Allele/Variant
Source: rs257356790
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112192834C>T

Allele/Variant
Source: rs244128218
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112193398G>A

Allele/Variant
Source: rs580190549
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112203117T>A

Allele/Variant
Source: rs242469548
Genes: Wdr59 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)8:112190490G>A