Version: 8.0.0
Date: Tue Jan 28 2025
112 results
Allele/Variant Genes: Pgap4 (Rno)

(mRatBN7.2)5:63933588G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320415799
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63933588G>A

(mRatBN7.2)5:63933273G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197710387
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63933273G>A

(mRatBN7.2)5:63949154A>C

(Rattus norvegicus)
Allele/Variant
Source: rs198842047
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63949154A>C

(mRatBN7.2)5:63935673G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320576168
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63935673G>A

(mRatBN7.2)5:63936580T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320415729
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63936580T>A

(mRatBN7.2)5:63939126A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105389096
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63939126A>G

(mRatBN7.2)5:63930794A>T

(Rattus norvegicus)
Allele/Variant
Source: rs198010100
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63930794A>T

(mRatBN7.2)5:63941498T>A

(Rattus norvegicus)
Allele/Variant
Source: rs107530933
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63941498T>A

(mRatBN7.2)5:63943212G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320514303
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63943212G>A

(mRatBN7.2)5:63943812C>A

(Rattus norvegicus)
Allele/Variant
Source: rs106456479
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63943812C>A

(mRatBN7.2)5:63933194A>T

(Rattus norvegicus)
Allele/Variant
Source: rs199409656
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63933194A>T

(mRatBN7.2)5:63932574A>T

(Rattus norvegicus)
Allele/Variant
Source: rs13449472
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63932574A>T

(mRatBN7.2)5:63932022C>A

(Rattus norvegicus)
Allele/Variant
Source: rs8145036
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63932022C>A

(mRatBN7.2)5:63943343G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198627402
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63943343G>A

(mRatBN7.2)5:63949246C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197779247
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63949246C>T

(mRatBN7.2)5:63949419A>T

(Rattus norvegicus)
Allele/Variant
Source: rs197030785
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63949419A>T

(mRatBN7.2)5:63948929G>C

(Rattus norvegicus)
Allele/Variant
Source: rs105608992
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63948929G>C

(mRatBN7.2)5:63933792C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197110762
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63933792C>T

(mRatBN7.2)5:63934299A>G

(Rattus norvegicus)
Allele/Variant
Source: rs199143073
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63934299A>G

(mRatBN7.2)5:63949732C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197347841
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63949732C>T

(mRatBN7.2)5:63950240G>A

(Rattus norvegicus)
Allele/Variant
Source: rs199263811
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63950240G>A

(mRatBN7.2)5:63947748T>G

(Rattus norvegicus)
Allele/Variant
Source: rs106604646
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63947748T>G

(mRatBN7.2)5:63938115G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320485621
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63938115G>T

(mRatBN7.2)5:63932040A>G

(Rattus norvegicus)
Allele/Variant
Source: rs199226434
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63932040A>G

(mRatBN7.2)5:63932502A>C

(Rattus norvegicus)
Allele/Variant
Source: rs106067436
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63932502A>C

(mRatBN7.2)5:63949213A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198155969
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63949213A>G

(mRatBN7.2)5:63950385T>C

(Rattus norvegicus)
Allele/Variant
Source: rs197935264
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63950385T>C

(mRatBN7.2)5:63950402A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198664554
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63950402A>G

(mRatBN7.2)5:63950448G>T

(Rattus norvegicus)
Allele/Variant
Source: rs198014928
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63950448G>T

(mRatBN7.2)5:63951108G>T

(Rattus norvegicus)
Allele/Variant
Source: rs198535923
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63951108G>T

(mRatBN7.2)5:63935505A>T

(Rattus norvegicus)
Allele/Variant
Source: rs107224891
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63935505A>T

(mRatBN7.2)5:63935605G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197934230
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63935605G>A

(mRatBN7.2)5:63935841C>G

(Rattus norvegicus)
Allele/Variant
Source: rs198065446
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63935841C>G

(mRatBN7.2)5:63949287T>C

(Rattus norvegicus)
Allele/Variant
Source: rs199098569
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63949287T>C

(mRatBN7.2)5:63935663T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320537310
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63935663T>G

(mRatBN7.2)5:63946508T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106749665
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63946508T>C

(mRatBN7.2)5:63947771A>T

(Rattus norvegicus)
Allele/Variant
Source: rs105888817
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63947771A>T

(mRatBN7.2)5:63948143A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198100343
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63948143A>G

(mRatBN7.2)5:63939086G>T

(Rattus norvegicus)
Allele/Variant
Source: rs105992359
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63939086G>T

(mRatBN7.2)5:63943925G>A

(Rattus norvegicus)
Allele/Variant
Source: rs107154869
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63943925G>A

(mRatBN7.2)5:63951436G>C

(Rattus norvegicus)
Allele/Variant
Source: rs198389313
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63951436G>C

(mRatBN7.2)5:63948112C>T

(Rattus norvegicus)
Allele/Variant
Source: rs199225409
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63948112C>T

(mRatBN7.2)5:63934902A>C

(Rattus norvegicus)
Allele/Variant
Source: rs198189073
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63934902A>C

(mRatBN7.2)5:63950185G>T

(Rattus norvegicus)
Allele/Variant
Source: rs197835100
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63950185G>T

(mRatBN7.2)5:63939766A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105580304
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63939766A>G

(mRatBN7.2)5:63934186A>T

(Rattus norvegicus)
Allele/Variant
Source: rs105602819
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63934186A>T

(mRatBN7.2)5:63943381G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105814216
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63943381G>A

(mRatBN7.2)5:63944333T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320576227
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63944333T>C

(mRatBN7.2)5:63937307T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051340.1:g.63937307T>A
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63937307T>A

(mRatBN7.2)5:63946612A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320560419
Genes: Pgap4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:63946612A>T