16 results
Allele/Variant Genes: Sap30 (Rno)

(mRatBN7.2)16:32749507T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322972886
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32749507T>C

(mRatBN7.2)16:32751919G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323035166
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32751919G>T

(mRatBN7.2)16:32750679T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322556552
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32750679T>C

(mRatBN7.2)16:32750005C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322791144
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32750005C>T

(mRatBN7.2)16:32751940A>C

(Rattus norvegicus)
Allele/Variant
Source: rs107356137
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32751940A>C

(mRatBN7.2)16:32748271G>C

(Rattus norvegicus)
Allele/Variant
Source: rs105960514
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32748271G>C

(mRatBN7.2)16:32748511T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322875638
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32748511T>C

(mRatBN7.2)16:32752877C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322921609
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32752877C>T

(mRatBN7.2)16:32750399T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322945145
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32750399T>A

(mRatBN7.2)16:32747791A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322924335
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32747791A>G

(mRatBN7.2)16:32748906T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051351.1:g.32748906T>C
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32748906T>C

(mRatBN7.2)16:32750173T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322816278
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32750173T>C

(mRatBN7.2)16:32750401G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322816172
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32750401G>A

(mRatBN7.2)16:32752310G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322985959
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32752310G>A

(mRatBN7.2)16:32752684A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322921584
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32752684A>T

(mRatBN7.2)16:32748675T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322918699
Genes: Sap30 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)16:32748675T>G