Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: Trpv1 (Rno)
Trpv1em1Sage
(Rattus norvegicus)Allele/Variant
Source: RGD:13792702
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: myocardial infarction
Variant Name: Not Available
(mRatBN7.2)10:57852188A>T
(Rattus norvegicus)Allele/Variant
Source: rs3321753164
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57852188A>T
(mRatBN7.2)10:57852500A>G
(Rattus norvegicus)Allele/Variant
Source: rs8160549
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57852500A>G
(mRatBN7.2)10:57853993A>C
(Rattus norvegicus)Allele/Variant
Source: rs3321886337
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57853993A>C
(mRatBN7.2)10:57854036A>G
(Rattus norvegicus)Allele/Variant
Source: rs198557570
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57854036A>G
(mRatBN7.2)10:57854197C>T
(Rattus norvegicus)Allele/Variant
Source: rs3321860867
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57854197C>T
(mRatBN7.2)10:57856036C>T
(Rattus norvegicus)Allele/Variant
Source: rs3321581011
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57856036C>T
(mRatBN7.2)10:57856050T>C
(Rattus norvegicus)Allele/Variant
Source: rs197750832
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57856050T>C
(mRatBN7.2)10:57856302C>A
(Rattus norvegicus)Allele/Variant
Source: rs198741167
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57856302C>A
(mRatBN7.2)10:57857067C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.57857067C>T
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57857067C>T
(mRatBN7.2)10:57856895C>T
(Rattus norvegicus)Allele/Variant
Source: rs3321812814
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57856895C>T
(mRatBN7.2)10:57852187G>T
(Rattus norvegicus)Allele/Variant
Source: rs3321865194
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57852187G>T
(mRatBN7.2)10:57854175A>G
(Rattus norvegicus)Allele/Variant
Source: rs198031901
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57854175A>G
(mRatBN7.2)10:57857895C>G
(Rattus norvegicus)Allele/Variant
Source: rs198948772
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57857895C>G
(mRatBN7.2)10:57853993A>T
(Rattus norvegicus)Allele/Variant
Source: rs3321886337
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57853993A>T
(mRatBN7.2)10:57855093C>A
(Rattus norvegicus)Allele/Variant
Source: rs3321812820
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57855093C>A
(mRatBN7.2)10:57855381G>A
(Rattus norvegicus)Allele/Variant
Source: rs105577830
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57855381G>A
(mRatBN7.2)10:57858079A>G
(Rattus norvegicus)Allele/Variant
Source: rs3321841095
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57858079A>G
(mRatBN7.2)10:57858094C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.57858094C>T
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57858094C>T
(mRatBN7.2)10:57858144C>T
(Rattus norvegicus)Allele/Variant
Source: rs197662974
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57858144C>T
(mRatBN7.2)10:57858164A>C
(Rattus norvegicus)Allele/Variant
Source: rs198477073
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57858164A>C
(mRatBN7.2)10:57857057T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.57857057T>C
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57857057T>C
(mRatBN7.2)10:57857898A>G
(Rattus norvegicus)Allele/Variant
Source: rs197743056
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57857898A>G
(mRatBN7.2)10:57851505C>A
(Rattus norvegicus)Allele/Variant
Source: rs8160554
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57851505C>A
(mRatBN7.2)10:57851787A>G
(Rattus norvegicus)Allele/Variant
Source: rs198051524
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57851787A>G
(mRatBN7.2)10:57851993G>C
(Rattus norvegicus)Allele/Variant
Source: rs199065535
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57851993G>C
(mRatBN7.2)10:57852189G>T
(Rattus norvegicus)Allele/Variant
Source: rs3321753106
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57852189G>T
(mRatBN7.2)10:57854646G>A
(Rattus norvegicus)Allele/Variant
Source: rs198737268
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57854646G>A
(mRatBN7.2)10:57855114G>A
(Rattus norvegicus)Allele/Variant
Source: rs198714551
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57855114G>A
(mRatBN7.2)10:57856937T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.57856937T>C
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57856937T>C
(mRatBN7.2)10:57856965T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.57856965T>C
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57856965T>C
(mRatBN7.2)10:57858062C>T
(Rattus norvegicus)Allele/Variant
Source: rs3321844357
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57858062C>T
(mRatBN7.2)10:57859632C>T
(Rattus norvegicus)Allele/Variant
Source: rs196964588
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57859632C>T
(mRatBN7.2)10:57861599C>T
(Rattus norvegicus)Allele/Variant
Source: rs197586646
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57861599C>T
(mRatBN7.2)10:57864693C>A
(Rattus norvegicus)Allele/Variant
Source: rs197854162
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57864693C>A
(mRatBN7.2)10:57866120C>T
(Rattus norvegicus)Allele/Variant
Source: rs198408556
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57866120C>T
(mRatBN7.2)10:57867695C>T
(Rattus norvegicus)Allele/Variant
Source: rs198135323
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57867695C>T
(mRatBN7.2)10:57875750G>C
(Rattus norvegicus)Allele/Variant
Source: rs197309709
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57875750G>C
(mRatBN7.2)10:57875803G>A
(Rattus norvegicus)Allele/Variant
Source: rs198601556
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57875803G>A
(mRatBN7.2)10:57875815C>A
(Rattus norvegicus)Allele/Variant
Source: rs197525961
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57875815C>A
(mRatBN7.2)10:57875829C>T
(Rattus norvegicus)Allele/Variant
Source: rs198955956
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57875829C>T
(mRatBN7.2)10:57858866C>T
(Rattus norvegicus)Allele/Variant
Source: rs3321891798
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57858866C>T
(mRatBN7.2)10:57860134C>T
(Rattus norvegicus)Allele/Variant
Source: rs8160553
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57860134C>T
(mRatBN7.2)10:57862134T>C
(Rattus norvegicus)Allele/Variant
Source: rs8160548
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57862134T>C
(mRatBN7.2)10:57862646T>C
(Rattus norvegicus)Allele/Variant
Source: rs197389091
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57862646T>C
(mRatBN7.2)10:57863663A>G
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.57863663A>G
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57863663A>G
(mRatBN7.2)10:57864162G>A
(Rattus norvegicus)Allele/Variant
Source: rs3321886282
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57864162G>A
(mRatBN7.2)10:57868173G>A
(Rattus norvegicus)Allele/Variant
Source: rs199068402
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57868173G>A
(mRatBN7.2)10:57858113G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.57858113G>A
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57858113G>A
(mRatBN7.2)10:57858117G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051345.1:g.57858117G>A
Genes: Trpv1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:57858117G>A