113 results
Allele/Variant Genes: Nphp3 (Rno)

(mRatBN7.2)8:104626405C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321441699
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104626405C>G

(mRatBN7.2)8:104626843T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105327867
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104626843T>C

(mRatBN7.2)8:104633568C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321365216
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104633568C>T

(mRatBN7.2)8:104644770G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051343.1:g.104644770G>A
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104644770G>A

(mRatBN7.2)8:104646259C>G

(Rattus norvegicus)
Allele/Variant
Source: rs105126498
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104646259C>G

(mRatBN7.2)8:104647798C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105666085
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104647798C>T

(mRatBN7.2)8:104654459T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321217221
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104654459T>C

(mRatBN7.2)8:104654480G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321364948
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104654480G>A

(mRatBN7.2)8:104626605C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321415964
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104626605C>T

(mRatBN7.2)8:104626673A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106047498
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104626673A>G

(mRatBN7.2)8:104630358A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321333868
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104630358A>G

(mRatBN7.2)8:104631231C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105190524
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104631231C>T

(mRatBN7.2)8:104635325G>T

(Rattus norvegicus)
Allele/Variant
Source: rs105060221
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104635325G>T

(mRatBN7.2)8:104647858G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105537518
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104647858G>A

(mRatBN7.2)8:104658121T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105874538
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104658121T>C

(mRatBN7.2)8:104631232A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105954975
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104631232A>G

(mRatBN7.2)8:104631448A>C

(Rattus norvegicus)
Allele/Variant
Source: rs105639930
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104631448A>C

(mRatBN7.2)8:104646273G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321415863
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104646273G>A

(mRatBN7.2)8:104659409T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321442755
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104659409T>A

(mRatBN7.2)8:104660621G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321415921
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104660621G>A

(mRatBN7.2)8:104625348G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321377363
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104625348G>A

(mRatBN7.2)8:104626165T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106486215
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104626165T>C

(mRatBN7.2)8:104635038G>T

(Rattus norvegicus)
Allele/Variant
Source: rs107401668
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104635038G>T

(mRatBN7.2)8:104644771A>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051343.1:g.104644771A>T
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104644771A>T

(mRatBN7.2)8:104656735G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321510880
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104656735G>A

rs198028745

(Rattus norvegicus)
Allele/Variant
Source: rs198028745
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available

(mRatBN7.2)8:104661350C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321456389
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104661350C>G

(mRatBN7.2)8:104626805C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321377419
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104626805C>T

(mRatBN7.2)8:104631937A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105838480
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104631937A>G

(mRatBN7.2)8:104636927G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051343.1:g.104636927G>A
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104636927G>A

(mRatBN7.2)8:104627743G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106202039
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104627743G>A

(mRatBN7.2)8:104628292C>G

(Rattus norvegicus)
Allele/Variant
Source: rs105959540
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104628292C>G

(mRatBN7.2)8:104638980A>C

(Rattus norvegicus)
Allele/Variant
Source: rs199015370
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104638980A>C

(mRatBN7.2)8:104639845A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321333803
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104639845A>G

(mRatBN7.2)8:104648257G>A

(Rattus norvegicus)
Allele/Variant
Source: rs107569560
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104648257G>A

(mRatBN7.2)8:104648402C>A

(Rattus norvegicus)
Allele/Variant
Source: rs106212625
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104648402C>A

(mRatBN7.2)8:104656751T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321440976
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104656751T>C

(mRatBN7.2)8:104660734C>G

(Rattus norvegicus)
Allele/Variant
Source: rs199199253
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104660734C>G

(mRatBN7.2)8:104629203A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106745359
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104629203A>G

(mRatBN7.2)8:104634527A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3321441653
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104634527A>G

(mRatBN7.2)8:104627549A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106975017
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104627549A>G

(mRatBN7.2)8:104629212G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3321442927
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104629212G>A

(mRatBN7.2)8:104629640C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321480144
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104629640C>T

(mRatBN7.2)8:104630381C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105849713
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104630381C>T

(mRatBN7.2)8:104637519G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051343.1:g.104637519G>A
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104637519G>A

(mRatBN7.2)8:104646533C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3321333807
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104646533C>T

(mRatBN7.2)8:104658342A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105799496
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104658342A>G

(mRatBN7.2)8:104625772A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321440918
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104625772A>C

(mRatBN7.2)8:104626397T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321377306
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104626397T>C

(mRatBN7.2)8:104636771A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105384719
Genes: Nphp3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)8:104636771A>G