145 results
Allele/Variant Genes: C1qb (Mmu)

C1qbtm1(KOMP)Vlcg

(Mus musculus)
Allele/Variant
Source: MGI:5085493
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

C1qbem1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7462046
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

C1qbem3Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7296081
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

C1qbem1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7288553
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

C1qbtm1.1(KOMP)Vlcg

(Mus musculus)
Allele/Variant
Source: MGI:5471254
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

C1qbem1Cya

(Mus musculus)
Allele/Variant
Source: MGI:7582651
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs13473141
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136609487A>G

Allele/Variant
Source: rs251279789
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136611798T>C

Allele/Variant
Source: rs214506926
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136611802T>C

Allele/Variant
Source: rs27625306
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136607744C>T

Allele/Variant
Source: rs51073789
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136608791C>T

Allele/Variant
Source: rs235577749
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136613458C>T

Allele/Variant
Source: rs32197767
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136611810T>A

Allele/Variant
Source: rs27625284
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136612531G>A

Allele/Variant
Source: rs212870570
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136610962T>C

Allele/Variant
Source: rs581276576
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136611479A>G

Allele/Variant
Source: rs233972651
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136610309C>T

Allele/Variant
Source: rs27625290
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136610758G>A

Allele/Variant
Source: rs255108136
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136610841C>T

Allele/Variant
Source: rs233884117
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136611244A>G

Allele/Variant
Source: rs230276457
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136608424C>T

Allele/Variant
Source: rs264314268
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136609943C>T

Allele/Variant
Source: rs252822152
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136609957C>T

Allele/Variant
Source: rs264293388
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136610211C>T

Allele/Variant
Source: rs50487379
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136613473A>G

Allele/Variant
Source: rs242254423
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136610960C>T

Allele/Variant
Source: rs49864646
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136608957C>T

Allele/Variant
Source: rs212808345
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136610187C>T

Allele/Variant
Source: rs251312163
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136610244G>A

Allele/Variant
Source: rs586708931
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136610413C>T

Allele/Variant
Source: rs266070002
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136610713G>A

Allele/Variant
Source: rs27625304
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136607855G>A

Allele/Variant
Source: rs27625303
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136608206G>A

Allele/Variant
Source: rs1134316644
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136608802C>A

Allele/Variant
Source: rs52427050
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136609862C>T

Allele/Variant
Source: rs27625287
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136612063G>A

Allele/Variant
Source: rs226469831
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136610644G>A

Allele/Variant
Source: rs248643047
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136610655C>A

Allele/Variant
Source: rs32699944
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136611500A>G

Allele/Variant
Source: rs49312807
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136609074T>C

Allele/Variant
Source: rs258168820
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136609340G>A

Allele/Variant
Source: rs259993068
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136612673A>G

Allele/Variant
Source: rs46072481
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136610131C>T

Allele/Variant
Source: rs32822209
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136611982C>T

Allele/Variant
Source: rs27625285
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136612149A>G

Allele/Variant
Source: rs254573992
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136612487G>A

Allele/Variant
Source: rs222720847
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136607903T>C

Allele/Variant
Source: rs27625301
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136608368C>G

Allele/Variant
Source: rs27625300
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136608472A>G

Allele/Variant
Source: rs50819172
Genes: C1qb (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:136608857C>T