Version: 8.0.0
Date: Tue Jan 28 2025
190 results
Allele/Variant Genes: Ube2h (Rno)

(mRatBN7.2)4:58856104A>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051339.1:g.58856104A>T
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58856104A>T

(mRatBN7.2)4:58894783A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320193697
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58894783A>G

(mRatBN7.2)4:58912298G>A

(Rattus norvegicus)
Allele/Variant
Source: rs196975053
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58912298G>A

(mRatBN7.2)4:58862504A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320193774
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58862504A>G

(mRatBN7.2)4:58881211A>G

(Rattus norvegicus)
Allele/Variant
Source: rs197972381
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58881211A>G

rs199074198

(Rattus norvegicus)
Allele/Variant
Source: rs199074198
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available

(mRatBN7.2)4:58923371T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320193784
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58923371T>C

(mRatBN7.2)4:58908253T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051339.1:g.58908253T>A
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58908253T>A

(mRatBN7.2)4:58912122C>T

(Rattus norvegicus)
Allele/Variant
Source: rs199220190
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58912122C>T

(mRatBN7.2)4:58915662T>G

(Rattus norvegicus)
Allele/Variant
Source: rs198540678
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58915662T>G

(mRatBN7.2)4:58847639T>A

(Rattus norvegicus)
Allele/Variant
Source: rs198710312
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58847639T>A

(mRatBN7.2)4:58885644A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320184191
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58885644A>C

(mRatBN7.2)4:58923985A>G

(Rattus norvegicus)
Allele/Variant
Source: rs197826472
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58923985A>G

(mRatBN7.2)4:58925723T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320144271
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58925723T>C

(mRatBN7.2)4:58902936C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198990251
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58902936C>T

(mRatBN7.2)4:58840687C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197173442
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58840687C>T

(mRatBN7.2)4:58911781G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051339.1:g.58911781G>A
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58911781G>A

(mRatBN7.2)4:58849144A>G

(Rattus norvegicus)
Allele/Variant
Source: rs197794422
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58849144A>G

(mRatBN7.2)4:58859423C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197828090
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58859423C>T

(mRatBN7.2)4:58859888C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197157439
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58859888C>T

(mRatBN7.2)4:58876428T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051339.1:g.58876428T>C
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58876428T>C

(mRatBN7.2)4:58913191G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051339.1:g.58913191G>A
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58913191G>A

(mRatBN7.2)4:58847216C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320201811
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58847216C>T

(mRatBN7.2)4:58898111G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320193728
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58898111G>A

(mRatBN7.2)4:58909283A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051339.1:g.58909283A>G
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58909283A>G

(mRatBN7.2)4:58911433G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051339.1:g.58911433G>A
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58911433G>A

(mRatBN7.2)4:58914639T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320184184
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58914639T>C

(mRatBN7.2)4:58915713G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198094328
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58915713G>A

(mRatBN7.2)4:58915717A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198878604
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58915717A>G

(mRatBN7.2)4:58842712C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320144289
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58842712C>T

(mRatBN7.2)4:58859197A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320124895
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58859197A>C

(mRatBN7.2)4:58866490G>C

(Rattus norvegicus)
Allele/Variant
Source: rs199320471
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58866490G>C

(mRatBN7.2)4:58886975G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320068710
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58886975G>T

(mRatBN7.2)4:58889741C>G

(Rattus norvegicus)
Allele/Variant
Source: rs104913783
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58889741C>G

(mRatBN7.2)4:58891297A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198843251
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58891297A>G

(mRatBN7.2)4:58859201A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320181259
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58859201A>C

(mRatBN7.2)4:58915721G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320124940
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58915721G>A

(mRatBN7.2)4:58904180G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197917316
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58904180G>A

(mRatBN7.2)4:58847383G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320150400
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58847383G>A

(mRatBN7.2)4:58906398A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051339.1:g.58906398A>G
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58906398A>G

(mRatBN7.2)4:58849611A>G

(Rattus norvegicus)
Allele/Variant
Source: rs107492384
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58849611A>G

(mRatBN7.2)4:58890299G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320144325
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58890299G>A

(mRatBN7.2)4:58893747G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198371524
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58893747G>A

(mRatBN7.2)4:58925724G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320215483
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58925724G>C

(mRatBN7.2)4:58903698A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320181199
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58903698A>G

(mRatBN7.2)4:58904669A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051339.1:g.58904669A>G
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58904669A>G

(mRatBN7.2)4:58849746G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320144301
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58849746G>A

(mRatBN7.2)4:58859303T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320181258
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58859303T>G

(mRatBN7.2)4:58859410C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198449983
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58859410C>T

(mRatBN7.2)4:58870599C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320150535
Genes: Ube2h (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:58870599C>T