2,005 results
Allele/Variant Genes: Cfap57 (Mmu)

Cfap57em1(IMPC)Mbp

(Mus musculus)
Allele/Variant
Source: MGI:6152429
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Cfap57em1Qsh

(Mus musculus)
Allele/Variant
Source: MGI:7529021
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: splice_region_variant, frameshift_variant
Diseases: male infertility
Variant Name: Not Available

Allele/Variant
Source: rs254813606
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118414663T>A

Allele/Variant
Source: rs260664086
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118415088C>T

Allele/Variant
Source: rs233125210
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118415408C>A

Allele/Variant
Source: rs27510978
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118415516C>T

Allele/Variant
Source: rs253468617
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118415621C>T

Allele/Variant
Source: rs234210658
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118416538A>C

Allele/Variant
Source: rs230349540
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118415736C>T

Allele/Variant
Source: rs247637127
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118415795T>C

Allele/Variant
Source: rs27510973
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118415875A>G

Allele/Variant
Source: rs224473615
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118416017C>T

Allele/Variant
Source: rs585579530
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118468066G>A

Allele/Variant
Source: rs256501176
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118416057C>T

Allele/Variant
Source: rs578712376
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118416125G>A

Allele/Variant
Source: rs230348418
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118422906C>T

Allele/Variant
Source: rs216567797
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118423894C>A

Allele/Variant
Source: rs215673405
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118418494C>T

Allele/Variant
Source: rs235062973
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118424714C>T

Allele/Variant
Source: rs238069802
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118424786T>C

Allele/Variant
Source: rs223657691
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118425046G>C

Allele/Variant
Source: rs222894737
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118425081C>T

Allele/Variant
Source: rs580807986
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118414213T>G

Allele/Variant
Source: rs586732771
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118414249G>A

Allele/Variant
Source: rs232850981
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118412671G>A

Allele/Variant
Source: rs27510965
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118418172A>T

Allele/Variant
Source: rs27510964
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118418181T>C

Allele/Variant
Source: rs256165730
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118418351C>T

Allele/Variant
Source: rs260874479
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118423300G>C

Allele/Variant
Source: rs224352293
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118424118G>T

Allele/Variant
Source: rs250346504
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118424486T>C

Allele/Variant
Source: rs45979990
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118425139G>A

Allele/Variant
Source: rs580203904
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118413125G>A

Allele/Variant
Source: rs227454221
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118414497G>A

Allele/Variant
Source: rs227269608
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118418511T>C

Allele/Variant
Source: rs250671375
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118418793A>G

Allele/Variant
Source: rs217374068
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118420041C>T

Allele/Variant
Source: rs579793662
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118418407T>A

Allele/Variant
Source: rs246080869
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118417518A>C

Allele/Variant
Source: rs234987326
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118417553A>G

Allele/Variant
Source: rs212305782
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118421585G>A

Allele/Variant
Source: rs1132868381
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118422113G>A

Allele/Variant
Source: rs580739661
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118416099G>A

Allele/Variant
Source: rs258579187
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118416124C>G

Allele/Variant
Source: rs230291595
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118416305A>G

Allele/Variant
Source: rs243465029
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118416279A>G

Allele/Variant
Source: rs238617241
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118419235G>T

Allele/Variant
Source: rs27510960
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118419743T>C

Allele/Variant
Source: rs263091103
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118419779C>A

Allele/Variant
Source: rs248197216
Genes: Cfap57 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:118423126G>T