16 results
Allele/Variant Genes: Clec3b (Rno)

(mRatBN7.2)8:122810688C>T

(Rattus norvegicus)
Allele/Variant
Source: rs199051401
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122810688C>T

(mRatBN7.2)8:122810900T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106616923
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122810900T>C

(mRatBN7.2)8:122812731A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198152781
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122812731A>G

(mRatBN7.2)8:122810446T>C

(Rattus norvegicus)
Allele/Variant
Source: rs107426144
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122810446T>C

(mRatBN7.2)8:122812751A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051343.1:g.122812751A>G
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122812751A>G

(mRatBN7.2)8:122811467T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321480014
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122811467T>C

(mRatBN7.2)8:122813373G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321402957
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122813373G>T

(mRatBN7.2)8:122812433A>T

(Rattus norvegicus)
Allele/Variant
Source: rs199158844
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122812433A>T

(mRatBN7.2)8:122814047A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105812705
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122814047A>G

(mRatBN7.2)8:122812708C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321553441
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122812708C>T

(mRatBN7.2)8:122812982G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198525388
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122812982G>A

(mRatBN7.2)8:122814206C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321253526
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122814206C>T

(mRatBN7.2)8:122815701G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321523527
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122815701G>A

(mRatBN7.2)8:122810782G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321416554
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122810782G>A

(mRatBN7.2)8:122812728C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197616516
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122812728C>T

(mRatBN7.2)8:122810989G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321494496
Genes: Clec3b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:122810989G>A