495 results
Allele/Variant Genes: Wbp2nl (Mmu)

Wbp2nltm1.1Osb

(Mus musculus)
Allele/Variant
Source: MGI:5882390
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Wbp2nlem15Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7308577
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Wbp2nlem1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7308578
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Wbp2nlem1(IMPC)Mbp

(Mus musculus)
Allele/Variant
Source: MGI:6152677
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Wbp2nltm1Osb

(Mus musculus)
Allele/Variant
Source: MGI:6759003
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs585448163
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82190865C>T

Allele/Variant
Source: rs586064000
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82190924G>A

Allele/Variant
Source: rs245546184
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82192981G>A

Allele/Variant
Source: rs232150496
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82194260T>C

Allele/Variant
Source: rs260635839
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82196909C>G

Allele/Variant
Source: rs31683576
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82198717G>C

Allele/Variant
Source: rs585129819
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82184390G>T

Allele/Variant
Source: rs580898269
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82184400G>T

Allele/Variant
Source: rs239399305
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82184419T>C

Allele/Variant
Source: rs31682583
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82184618A>G

Allele/Variant
Source: rs259469975
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82193387T>G

Allele/Variant
Source: rs264578888
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82198373G>A

Allele/Variant
Source: rs235004835
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82183485G>A

Allele/Variant
Source: rs586482058
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82185180G>A

Allele/Variant
Source: rs31683612
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82185212G>A

Allele/Variant
Source: rs583063501
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82186662A>G

Allele/Variant
Source: rs225887759
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82187853A>T

Allele/Variant
Source: rs263500769
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82191494T>A

Allele/Variant
Source: rs1135217295
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82191649T>A

Allele/Variant
Source: rs261469356
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82191712C>T

Allele/Variant
Source: rs217365239
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82183636A>G

Allele/Variant
Source: rs583711263
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82183772A>T

Allele/Variant
Source: rs31683608
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82184795A>C

Allele/Variant
Source: rs578842769
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82185053G>T

Allele/Variant
Source: rs234196116
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82185071A>G

Allele/Variant
Source: rs31684564
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82185247T>G

Allele/Variant
Source: rs250522447
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82186964G>A

Allele/Variant
Source: rs258291018
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82189656G>A

Allele/Variant
Source: rs251000968
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82190120A>G

Allele/Variant
Source: rs1133822207
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82194684T>C

Allele/Variant
Source: rs223700085
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82185271C>A

Allele/Variant
Source: rs231499283
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82183563G>A

Allele/Variant
Source: rs224201827
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82184749C>G

Allele/Variant
Source: rs231828986
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82185936G>A

Allele/Variant
Source: rs260306524
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82188250T>G

Allele/Variant
Source: rs231541557
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82188965A>G

Allele/Variant
Source: rs212491709
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82188988T>G

Allele/Variant
Source: rs233612125
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82193378A>G

Allele/Variant
Source: rs1133100560
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82194778T>C

Allele/Variant
Source: rs249270225
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82185559A>G

Allele/Variant
Source: rs265514075
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82185166G>A

Allele/Variant
Source: rs249692677
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82185967T>C

Allele/Variant
Source: rs212886232
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82185984A>C

Allele/Variant
Source: rs262991373
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82186161C>T

Allele/Variant
Source: rs238993356
Genes: Wbp2nl (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:82186237G>A