Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: Nox1 (Rno)
(mRatBN7.2)X:97290586C>T
(Rattus norvegicus)Allele/Variant
Source: rs3323648708
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97290586C>T
(mRatBN7.2)X:97298004A>G
(Rattus norvegicus)Allele/Variant
Source: rs3323692253
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97298004A>G
(mRatBN7.2)X:97302055C>T
(Rattus norvegicus)Allele/Variant
Source: rs3323668599
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97302055C>T
(mRatBN7.2)X:97322694A>C
(Rattus norvegicus)Allele/Variant
Source: rs65421093
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97322694A>C
(mRatBN7.2)X:97322700A>C
(Rattus norvegicus)Allele/Variant
Source: rs198898294
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97322700A>C
(mRatBN7.2)X:97324072T>C
(Rattus norvegicus)Allele/Variant
Source: NC_051356.1:g.97324072T>C
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97324072T>C
(mRatBN7.2)X:97324918C>T
(Rattus norvegicus)Allele/Variant
Source: NC_051356.1:g.97324918C>T
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97324918C>T
(mRatBN7.2)X:97325681T>C
(Rattus norvegicus)Allele/Variant
Source: rs3323673711
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97325681T>C
(mRatBN7.2)X:97323138G>A
(Rattus norvegicus)Allele/Variant
Source: rs197657156
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97323138G>A
(mRatBN7.2)X:97328507C>T
(Rattus norvegicus)Allele/Variant
Source: rs3323648771
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97328507C>T
(mRatBN7.2)X:97307707A>G
(Rattus norvegicus)Allele/Variant
Source: rs3323700987
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97307707A>G
(mRatBN7.2)X:97314266T>G
(Rattus norvegicus)Allele/Variant
Source: rs3323668454
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97314266T>G
(mRatBN7.2)X:97323136C>A
(Rattus norvegicus)Allele/Variant
Source: rs199341308
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97323136C>A
(mRatBN7.2)X:97323406C>G
(Rattus norvegicus)Allele/Variant
Source: rs197203159
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97323406C>G
(mRatBN7.2)X:97323727G>A
(Rattus norvegicus)Allele/Variant
Source: rs3323471204
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97323727G>A
(mRatBN7.2)X:97293925G>A
(Rattus norvegicus)Allele/Variant
Source: rs3323519383
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97293925G>A
(mRatBN7.2)X:97298566T>C
(Rattus norvegicus)Allele/Variant
Source: rs3323668613
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97298566T>C
(mRatBN7.2)X:97316305A>C
(Rattus norvegicus)Allele/Variant
Source: NC_051356.1:g.97316305A>C
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97316305A>C
(mRatBN7.2)X:97328476T>C
(Rattus norvegicus)Allele/Variant
Source: rs3323734840
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97328476T>C
(mRatBN7.2)X:97329572G>A
(Rattus norvegicus)Allele/Variant
Source: NC_051356.1:g.97329572G>A
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97329572G>A
(mRatBN7.2)X:97285404A>G
(Rattus norvegicus)Allele/Variant
Source: rs3323668556
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97285404A>G
rs3318805940
(Rattus norvegicus)Allele/Variant
Source: rs3318805940
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available
(mRatBN7.2)X:97329024T>A
(Rattus norvegicus)Allele/Variant
Source: rs3323641363
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97329024T>A
(mRatBN7.2)X:97330736G>A
(Rattus norvegicus)Allele/Variant
Source: rs3323714418
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97330736G>A
(mRatBN7.2)X:97330923A>C
(Rattus norvegicus)Allele/Variant
Source: rs3323641616
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97330923A>C
(mRatBN7.2)X:97302056G>A
(Rattus norvegicus)Allele/Variant
Source: rs3323673705
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97302056G>A
(mRatBN7.2)X:97306290C>T
(Rattus norvegicus)Allele/Variant
Source: rs3323602741
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97306290C>T
(mRatBN7.2)X:97325669G>A
(Rattus norvegicus)Allele/Variant
Source: rs3323249733
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97325669G>A
(mRatBN7.2)X:97326878T>A
(Rattus norvegicus)Allele/Variant
Source: rs3323668533
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97326878T>A
(mRatBN7.2)X:97330886C>T
(Rattus norvegicus)Allele/Variant
Source: rs3323648652
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97330886C>T
(mRatBN7.2)X:97326110G>A
(Rattus norvegicus)Allele/Variant
Source: rs3323471163
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97326110G>A
(mRatBN7.2)X:97328294T>A
(Rattus norvegicus)Allele/Variant
Source: rs3323641559
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97328294T>A
(mRatBN7.2)X:97326408T>C
(Rattus norvegicus)Allele/Variant
Source: rs3323641380
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97326408T>C
(mRatBN7.2)X:97328857T>C
(Rattus norvegicus)Allele/Variant
Source: rs3323668709
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97328857T>C
(mRatBN7.2)X:97330988T>C
(Rattus norvegicus)Allele/Variant
Source: rs3323648735
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97330988T>C
(mRatBN7.2)X:97294579A>G
(Rattus norvegicus)Allele/Variant
Source: rs3323545731
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97294579A>G
(mRatBN7.2)X:97297067C>T
(Rattus norvegicus)Allele/Variant
Source: rs3323471193
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97297067C>T
(mRatBN7.2)X:97306065G>A
(Rattus norvegicus)Allele/Variant
Source: rs3323734786
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97306065G>A
(mRatBN7.2)X:97307875G>A
(Rattus norvegicus)Allele/Variant
Source: rs3323700962
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97307875G>A
(mRatBN7.2)X:97308006G>C
(Rattus norvegicus)Allele/Variant
Source: rs3323471080
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97308006G>C
(mRatBN7.2)X:97286431G>A
(Rattus norvegicus)Allele/Variant
Source: rs3323648983
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97286431G>A
(mRatBN7.2)X:97293471C>A
(Rattus norvegicus)Allele/Variant
Source: NC_051356.1:g.97293471C>A
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97293471C>A
(mRatBN7.2)X:97308008C>A
(Rattus norvegicus)Allele/Variant
Source: rs3323700969
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97308008C>A
(mRatBN7.2)X:97309064T>G
(Rattus norvegicus)Allele/Variant
Source: rs3323705969
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97309064T>G
(mRatBN7.2)X:97323598C>T
(Rattus norvegicus)Allele/Variant
Source: rs3323692262
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97323598C>T
(mRatBN7.2)X:97326038A>G
(Rattus norvegicus)Allele/Variant
Source: rs3323673527
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97326038A>G
(mRatBN7.2)X:97279923C>T
(Rattus norvegicus)Allele/Variant
Source: rs3323712030
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97279923C>T
(mRatBN7.2)X:97297053A>T
(Rattus norvegicus)Allele/Variant
Source: rs3323692321
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97297053A>T
(mRatBN7.2)X:97301884T>C
(Rattus norvegicus)Allele/Variant
Source: rs3323545745
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97301884T>C
(mRatBN7.2)X:97302991T>G
(Rattus norvegicus)Allele/Variant
Source: NC_051356.1:g.97302991T>G
Genes: Nox1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)X:97302991T>G