47 results
Allele/Variant Genes: Ccl8 (Mmu)

Ccl8tm1b(KOMP)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:5548325
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl8em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7296440
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl8tm1a(KOMP)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:4419454
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl8em2Cya

(Mus musculus)
Allele/Variant
Source: MGI:7582789
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl8em2Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7645484
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl8em1Cya

(Mus musculus)
Allele/Variant
Source: MGI:7582788
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl8tm1c(KOMP)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:6856602
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl8em1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7288714
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs214926814
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006669C>T

Allele/Variant
Source: rs28207539
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82007532T>G

Allele/Variant
Source: rs219180519
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006723C>A

Allele/Variant
Source: rs245550041
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006647G>A

Allele/Variant
Source: rs232007090
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006837C>G

Allele/Variant
Source: rs1132008217
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82007557C>T

Allele/Variant
Source: rs28207547
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006099A>G

Allele/Variant
Source: rs28207545
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006266C>A

Allele/Variant
Source: rs257400400
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006327G>T

Allele/Variant
Source: rs1131741619
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006409G>A

Allele/Variant
Source: rs28207540
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82007164A>G

Allele/Variant
Source: rs227873475
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82007380C>T

Allele/Variant
Source: rs28207548
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006021T>C

Allele/Variant
Source: rs250259380
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006596C>T

Allele/Variant
Source: rs221992772
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006796C>T

Allele/Variant
Source: rs220506871
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82007078G>A

Allele/Variant
Source: rs247779249
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82007487C>T

Allele/Variant
Source: rs28207546
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006215T>C

Allele/Variant
Source: rs240915502
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006927A>C

Allele/Variant
Source: rs240760202
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82007289A>G

Allele/Variant
Source: rs240875781
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006461A>G

Allele/Variant
Source: rs28207544
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006496G>A

Allele/Variant
Source: rs247660905
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006711A>G

Allele/Variant
Source: rs28207543
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006729A>G

Allele/Variant
Source: rs221535750
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006904T>A

Allele/Variant
Source: rs261417833
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006107C>T

Allele/Variant
Source: rs228688235
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006540T>C

Allele/Variant
Source: rs231145923
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006614C>T

Allele/Variant
Source: rs265156882
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006608G>A

Allele/Variant
Source: rs256251951
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006742C>T

Allele/Variant
Source: rs226847155
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82007286G>A

Allele/Variant
Source: rs585005735
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006528T>C

Allele/Variant
Source: rs28207542
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006892A>G

Allele/Variant
Source: rs264283801
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006936G>A

Allele/Variant
Source: rs258884646
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82007369A>G

Allele/Variant
Source: rs221509533
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006363C>T

Allele/Variant
Source: rs28207541
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82007093G>A

Allele/Variant
Source: rs234470942
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82006671C>T

Allele/Variant
Source: rs28207538
Genes: Ccl8 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:82007605T>C