Version: 8.0.0
Date: Tue Jan 28 2025
571 results
Allele/Variant Genes: Gnaq (Rno)

(mRatBN7.2)1:213585495A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319157713
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213585495A>G

(mRatBN7.2)1:213621531T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319200337
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213621531T>C

(mRatBN7.2)1:213640812T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319197718
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213640812T>G

(mRatBN7.2)1:213626438C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213626438C>T
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213626438C>T

(mRatBN7.2)1:213462312C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319200482
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213462312C>G

(mRatBN7.2)1:213544226G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105353733
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213544226G>A

(mRatBN7.2)1:213607457C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319198495
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213607457C>T

(mRatBN7.2)1:213611060A>C

(Rattus norvegicus)
Allele/Variant
Source: rs105290048
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213611060A>C

(mRatBN7.2)1:213482776A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213482776A>G
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213482776A>G

(mRatBN7.2)1:213511443G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319191941
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213511443G>T

(mRatBN7.2)1:213432744G>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213432744G>T
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213432744G>T

(mRatBN7.2)1:213461473C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319196931
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213461473C>T

(mRatBN7.2)1:213475156G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213475156G>A
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213475156G>A

(mRatBN7.2)1:213476126G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213476126G>A
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213476126G>A

(mRatBN7.2)1:213477998C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213477998C>T
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213477998C>T

(mRatBN7.2)1:213480771T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213480771T>C
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213480771T>C

(mRatBN7.2)1:213592675T>G

(Rattus norvegicus)
Allele/Variant
Source: rs105739842
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213592675T>G

(mRatBN7.2)1:213595583G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319198452
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213595583G>A

(mRatBN7.2)1:213487764G>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213487764G>C
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213487764G>C

(mRatBN7.2)1:213666997G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319157838
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213666997G>A

(mRatBN7.2)1:213435727C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213435727C>T
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213435727C>T

(mRatBN7.2)1:213467145T>G

(Rattus norvegicus)
Allele/Variant
Source: rs104950949
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213467145T>G

(mRatBN7.2)1:213467983G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105600271
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213467983G>A

(mRatBN7.2)1:213535464G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106495272
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213535464G>A

(mRatBN7.2)1:213500372T>A

(Rattus norvegicus)
Allele/Variant
Source: rs105102789
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213500372T>A

(mRatBN7.2)1:213589533T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319157886
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213589533T>C

(mRatBN7.2)1:213589927G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319197798
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213589927G>A

(mRatBN7.2)1:213593661G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213593661G>A
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213593661G>A

(mRatBN7.2)1:213482972A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106873587
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213482972A>G

(mRatBN7.2)1:213487249T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213487249T>C
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213487249T>C

(mRatBN7.2)1:213432187C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213432187C>T
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213432187C>T

(mRatBN7.2)1:213435531G>T

(Rattus norvegicus)
Allele/Variant
Source: rs106870434
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213435531G>T

(mRatBN7.2)1:213503053T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106427746
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213503053T>C

(mRatBN7.2)1:213554052G>C

(Rattus norvegicus)
Allele/Variant
Source: rs66361795
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213554052G>C

(mRatBN7.2)1:213592417C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319196475
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213592417C>A

(mRatBN7.2)1:213488702A>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213488702A>C
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213488702A>C

(mRatBN7.2)1:213490075C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213490075C>T
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213490075C>T

(mRatBN7.2)1:213519212C>T

(Rattus norvegicus)
Allele/Variant
Source: rs104959412
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213519212C>T

(mRatBN7.2)1:213519718C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319198440
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213519718C>T

(mRatBN7.2)1:213522013G>A

(Rattus norvegicus)
Allele/Variant
Source: rs107364222
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213522013G>A

(mRatBN7.2)1:213514782A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3319201983
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213514782A>G

(mRatBN7.2)1:213651306C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213651306C>T
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213651306C>T

(mRatBN7.2)1:213555364C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319201937
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213555364C>T

(mRatBN7.2)1:213569592C>G

(Rattus norvegicus)
Allele/Variant
Source: rs105314169
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213569592C>G

(mRatBN7.2)1:213445622G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319202433
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213445622G>T

(mRatBN7.2)1:213449181C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319196344
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213449181C>T

(mRatBN7.2)1:213465676A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319197735
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213465676A>T

(mRatBN7.2)1:213477059T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.213477059T>A
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213477059T>A

(mRatBN7.2)1:213626456T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3319157867
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213626456T>C

(mRatBN7.2)1:213647850C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3319184684
Genes: Gnaq (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:213647850C>T