65 results
Allele/Variant Genes: Ccl2 (Mmu)

Ccl2tm1Rol

(Mus musculus)
Allele/Variant
Source: MGI:2175911
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: age related macular degeneration
Variant Name: Not Available

Ccl2tm1Dple

(Mus musculus)
Allele/Variant
Source: MGI:5636605
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl2tm1.1Jspa

(Mus musculus)
Allele/Variant
Source: MGI:7316776
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl2tm1Tyos

(Mus musculus)
Allele/Variant
Source: MGI:4355945
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl2em1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7643800
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl2tm1.2Tyos

(Mus musculus)
Allele/Variant
Source: MGI:5507824
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl2em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7296429
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl2em2Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7296430
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl2tm1.1Pame

(Mus musculus)
Allele/Variant
Source: MGI:4950271
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl2tm1Lex

(Mus musculus)
Allele/Variant
Source: MGI:5462245
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl2tm1.1Tyos

(Mus musculus)
Allele/Variant
Source: MGI:4355946
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Ccl2em2Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7645235
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs240837408
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927243G>A

Allele/Variant
Source: rs227483779
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926720A>C

Allele/Variant
Source: rs587259349
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926894A>G

Allele/Variant
Source: rs256910340
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927170G>A

Allele/Variant
Source: rs249727626
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927281C>T

Allele/Variant
Source: rs214408116
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927319C>T

Allele/Variant
Source: rs1132864478
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927722C>T

Allele/Variant
Source: rs213932038
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926723A>G

Allele/Variant
Source: rs580486220
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926888G>C

Allele/Variant
Source: rs215984805
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926918C>T

Allele/Variant
Source: rs583661470
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926890T>C

Allele/Variant
Source: rs235984668
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926931G>A

Allele/Variant
Source: rs261378355
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927064A>G

Allele/Variant
Source: rs582210762
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926416C>G

Allele/Variant
Source: rs585856893
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926448C>T

Allele/Variant
Source: rs28222413
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926518C>T

Allele/Variant
Source: rs266134104
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81928232T>C

Allele/Variant
Source: rs254411371
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926721A>C

Allele/Variant
Source: rs246671808
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926635T>C

Allele/Variant
Source: rs581092884
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926977T>A

Allele/Variant
Source: rs264398375
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927259A>G

Allele/Variant
Source: rs238022270
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926456C>A

Allele/Variant
Source: rs28222407
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927476A>G

Allele/Variant
Source: rs235575773
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927676C>T

Allele/Variant
Source: rs216014216
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927606C>A

Allele/Variant
Source: rs257397707
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927830T>C

Allele/Variant
Source: rs246947517
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81928227A>G

Allele/Variant
Source: rs28222409
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927373G>A

Allele/Variant
Source: rs28222406
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927832G>A

Allele/Variant
Source: rs232950893
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926899C>A

Allele/Variant
Source: rs212355030
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927729C>G

Allele/Variant
Source: rs221195161
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81928104G>A

Allele/Variant
Source: rs252865467
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926902G>A

Allele/Variant
Source: rs242463442
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927041T>A

Allele/Variant
Source: rs238156893
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927169T>G

Allele/Variant
Source: rs28222412
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81926676A>C

Allele/Variant
Source: rs28222410
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927209T>C

Allele/Variant
Source: rs228008521
Genes: Ccl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)11:81927265G>A