1,102 results
Allele/Variant Genes: Cpap (Mmu)

Cpaptm1a(EUCOMM)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:4432238
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Seckel syndrome
Variant Name: Not Available

Cpaptm1c(EUCOMM)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:5609807
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Cpaptm1d(EUCOMM)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:5613963
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Cpaptm1.1Tkt

(Mus musculus)
Allele/Variant
Source: MGI:5428007
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Cpaptm1b(EUCOMM)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:5609805
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs6299676
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56767741A>G

Allele/Variant
Source: rs1133241932
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56767941A>T

Allele/Variant
Source: rs31301165
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56770865T>A

Allele/Variant
Source: rs1132227718
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56778855G>A

Allele/Variant
Source: rs30144321
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56772472C>T

Allele/Variant
Source: rs587242209
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56779021A>G

Allele/Variant
Source: rs249767520
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56779246C>A

Allele/Variant
Source: rs261305628
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56795133G>A

Allele/Variant
Source: rs265157475
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56795146G>A

Allele/Variant
Source: rs257451697
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56791572T>C

Allele/Variant
Source: rs245173212
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56767135G>C

Allele/Variant
Source: rs1132240729
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56768800T>G

Allele/Variant
Source: rs233290481
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56769713T>C

Allele/Variant
Source: rs30604442
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56770673A>T

Allele/Variant
Source: rs238310602
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56770705C>T

Allele/Variant
Source: rs216042522
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56779355T>A

Allele/Variant
Source: rs262470044
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56779539G>A

Allele/Variant
Source: rs108271691
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56770850A>G

Allele/Variant
Source: rs1132143557
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56769495C>A

Allele/Variant
Source: rs580565789
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56769679A>C

Allele/Variant
Source: rs242466423
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56789709C>T

Allele/Variant
Source: rs232361043
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56789860T>A

Allele/Variant
Source: rs238667347
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56768014T>G

Allele/Variant
Source: rs258119937
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56768147G>T

Allele/Variant
Source: rs247326424
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56771084G>A

Allele/Variant
Source: rs232627916
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56771566T>C

Allele/Variant
Source: rs220920954
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56779564T>C

Allele/Variant
Source: rs221524060
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56779860G>T

Allele/Variant
Source: rs232664692
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56773149C>A

Allele/Variant
Source: rs1135046322
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56773927A>G

Allele/Variant
Source: rs260160706
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56766456T>C

Allele/Variant
Source: rs223380764
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56789971T>A

Allele/Variant
Source: rs262771456
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56792221G>T

Allele/Variant
Source: rs236631081
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56792682G>T

Allele/Variant
Source: rs583572577
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56793001A>C

Allele/Variant
Source: rs52275946
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56797767A>G

Allele/Variant
Source: rs214516413
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56798618A>C

Allele/Variant
Source: rs263602824
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56801405C>T

Allele/Variant
Source: rs235046585
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56800702G>T

Allele/Variant
Source: rs217612799
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56800745A>G

Allele/Variant
Source: rs240299830
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56793232T>C

Allele/Variant
Source: rs1134236511
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56793548G>A

Allele/Variant
Source: rs224752864
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56791016G>A

Allele/Variant
Source: rs217302154
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56789348A>C

Allele/Variant
Source: rs263661361
Genes: Cpap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:56794139A>G