Version: 8.0.0
Date: Tue Jan 28 2025
338 results
Allele/Variant Genes: Unc5b (Rno)

(mRatBN7.2)20:28711266A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323534293
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28711266A>G

(mRatBN7.2)20:28711349A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198070063
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28711349A>G

(mRatBN7.2)20:28711592C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106131840
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28711592C>T

(mRatBN7.2)20:28699260G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323599561
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28699260G>T

(mRatBN7.2)20:28754684G>C

(Rattus norvegicus)
Allele/Variant
Source: rs198880705
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28754684G>C

(mRatBN7.2)20:28757503A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105349810
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28757503A>G

(mRatBN7.2)20:28731513G>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051355.1:g.28731513G>C
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28731513G>C

(mRatBN7.2)20:28745649G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323423514
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28745649G>C

(mRatBN7.2)20:28747408G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323641289
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28747408G>C

(mRatBN7.2)20:28748617C>A

(Rattus norvegicus)
Allele/Variant
Source: rs199051693
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28748617C>A

(mRatBN7.2)20:28708946C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323423437
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28708946C>T

(mRatBN7.2)20:28699261A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323396569
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28699261A>T

(mRatBN7.2)20:28701347G>C

(Rattus norvegicus)
Allele/Variant
Source: rs105762978
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28701347G>C

(mRatBN7.2)20:28759180G>T

(Rattus norvegicus)
Allele/Variant
Source: rs107202824
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28759180G>T

(mRatBN7.2)20:28761109T>C

(Rattus norvegicus)
Allele/Variant
Source: rs197072054
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28761109T>C

(mRatBN7.2)20:28736367G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105263664
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28736367G>A

(mRatBN7.2)20:28736580C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323347237
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28736580C>T

(mRatBN7.2)20:28736729T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323541863
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28736729T>C

(mRatBN7.2)20:28739471A>G

(Rattus norvegicus)
Allele/Variant
Source: rs104901915
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28739471A>G

(mRatBN7.2)20:28742717A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323594144
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28742717A>T

(mRatBN7.2)20:28710202G>A

(Rattus norvegicus)
Allele/Variant
Source: rs199009489
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28710202G>A

(mRatBN7.2)20:28698605T>C

(Rattus norvegicus)
Allele/Variant
Source: rs199070522
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28698605T>C

(mRatBN7.2)20:28711850A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106578779
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28711850A>G

(mRatBN7.2)20:28712149G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323347242
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28712149G>A

(mRatBN7.2)20:28712513C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323541702
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28712513C>A

(mRatBN7.2)20:28712852G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106975634
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28712852G>A

(mRatBN7.2)20:28715124T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323396422
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28715124T>C

(mRatBN7.2)20:28720543A>G

(Rattus norvegicus)
Allele/Variant
Source: rs107446340
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28720543A>G

(mRatBN7.2)20:28760609T>A

(Rattus norvegicus)
Allele/Variant
Source: rs105085291
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28760609T>A

(mRatBN7.2)20:28710169C>A

(Rattus norvegicus)
Allele/Variant
Source: rs197910231
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28710169C>A

(mRatBN7.2)20:28713056C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323599338
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28713056C>T

(mRatBN7.2)20:28711636T>C

(Rattus norvegicus)
Allele/Variant
Source: rs107034527
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28711636T>C

(mRatBN7.2)20:28711643T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323594184
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28711643T>C

(mRatBN7.2)20:28701564T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105688538
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28701564T>C

(mRatBN7.2)20:28721945T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051355.1:g.28721945T>A
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28721945T>A

(mRatBN7.2)20:28751410T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3323566188
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28751410T>C

(mRatBN7.2)20:28728837T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105108595
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28728837T>C

(mRatBN7.2)20:28712084T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106221391
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28712084T>C

(mRatBN7.2)20:28711231T>C

(Rattus norvegicus)
Allele/Variant
Source: rs199129303
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28711231T>C

(mRatBN7.2)20:28711577C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323608413
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28711577C>T

(mRatBN7.2)20:28723830A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323486972
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28723830A>T

(mRatBN7.2)20:28761923A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106035805
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28761923A>G

(mRatBN7.2)20:28705940A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051355.1:g.28705940A>G
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28705940A>G

(mRatBN7.2)20:28697835T>C

(Rattus norvegicus)
Allele/Variant
Source: rs8153330
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28697835T>C

(mRatBN7.2)20:28698830T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106561867
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28698830T>C

(mRatBN7.2)20:28699283G>A

(Rattus norvegicus)
Allele/Variant
Source: rs197933418
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28699283G>A

(mRatBN7.2)20:28699602T>C

(Rattus norvegicus)
Allele/Variant
Source: rs107521989
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28699602T>C

(mRatBN7.2)20:28701793C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323641255
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28701793C>T

(mRatBN7.2)20:28703425G>T

(Rattus norvegicus)
Allele/Variant
Source: rs107217707
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28703425G>T

(mRatBN7.2)20:28703894T>G

(Rattus norvegicus)
Allele/Variant
Source: rs105822272
Genes: Unc5b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)20:28703894T>G