50 results
Allele/Variant Genes: Emc3 (Rno)

(mRatBN7.2)4:146671757G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320372726
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146671757G>A

(mRatBN7.2)4:146673347C>G

(Rattus norvegicus)
Allele/Variant
Source: rs197615514
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146673347C>G

(mRatBN7.2)4:146677394G>T

(Rattus norvegicus)
Allele/Variant
Source: rs105972889
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146677394G>T

(mRatBN7.2)4:146669449A>G

(Rattus norvegicus)
Allele/Variant
Source: rs198821102
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146669449A>G

(mRatBN7.2)4:146673979T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320383672
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146673979T>A

(mRatBN7.2)4:146663092A>T

(Rattus norvegicus)
Allele/Variant
Source: rs8147942
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146663092A>T

(mRatBN7.2)4:146673332C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106931103
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146673332C>T

(mRatBN7.2)4:146674449C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320382946
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146674449C>T

(mRatBN7.2)4:146677926G>T

(Rattus norvegicus)
Allele/Variant
Source: rs107581019
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146677926G>T

(mRatBN7.2)4:146669415G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320399711
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146669415G>C

(mRatBN7.2)4:146670878G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320325257
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146670878G>A

(mRatBN7.2)4:146678216G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051339.1:g.146678216G>A
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146678216G>A

(mRatBN7.2)4:146672128T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105496576
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146672128T>C

(mRatBN7.2)4:146673222A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320379846
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146673222A>G

(mRatBN7.2)4:146676347T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320228148
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146676347T>C

(mRatBN7.2)4:146663829C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320380024
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146663829C>T

(mRatBN7.2)4:146664206G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320372804
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146664206G>A

(mRatBN7.2)4:146664764T>A

(Rattus norvegicus)
Allele/Variant
Source: rs106918991
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146664764T>A

(mRatBN7.2)4:146667522C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320228170
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146667522C>T

(mRatBN7.2)4:146667825C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320383054
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146667825C>T

(mRatBN7.2)4:146665902C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320316203
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146665902C>T

(mRatBN7.2)4:146663439T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320372737
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146663439T>A

(mRatBN7.2)4:146667493C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320362561
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146667493C>T

(mRatBN7.2)4:146668752T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105961231
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146668752T>C

(mRatBN7.2)4:146675543A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320399767
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146675543A>C

(mRatBN7.2)4:146677397G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320298283
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146677397G>T

(mRatBN7.2)4:146674891C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197067077
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146674891C>T

(mRatBN7.2)4:146674901C>G

(Rattus norvegicus)
Allele/Variant
Source: rs198441666
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146674901C>G

(mRatBN7.2)4:146676519C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320372612
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146676519C>T

(mRatBN7.2)4:146674691T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320399603
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146674691T>G

(mRatBN7.2)4:146677257C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106751628
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146677257C>T

(mRatBN7.2)4:146677689C>G

(Rattus norvegicus)
Allele/Variant
Source: rs105532504
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146677689C>G

(mRatBN7.2)4:146664091T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320346000
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146664091T>C

(mRatBN7.2)4:146677766T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320316224
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146677766T>A

(mRatBN7.2)4:146665578G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320298324
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146665578G>T

(mRatBN7.2)4:146670984C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106683193
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146670984C>T

(mRatBN7.2)4:146668844T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320372811
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146668844T>A

(mRatBN7.2)4:146674472T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320387133
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146674472T>C

(mRatBN7.2)4:146664564C>A

(Rattus norvegicus)
Allele/Variant
Source: rs107210669
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146664564C>A

(mRatBN7.2)4:146673556C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320316151
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146673556C>T

(mRatBN7.2)4:146678385G>C

(Rattus norvegicus)
Allele/Variant
Source: rs105077150
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146678385G>C

(mRatBN7.2)4:146678394G>C

(Rattus norvegicus)
Allele/Variant
Source: rs104910200
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146678394G>C

(mRatBN7.2)4:146663490C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320228079
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146663490C>T

(mRatBN7.2)4:146663968T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106857566
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146663968T>C

(mRatBN7.2)4:146668095G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320362480
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146668095G>A

(mRatBN7.2)4:146668415C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320358968
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146668415C>T

(mRatBN7.2)4:146669408G>A

(Rattus norvegicus)
Allele/Variant
Source: rs106657482
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146669408G>A

(mRatBN7.2)4:146668375G>T

(Rattus norvegicus)
Allele/Variant
Source: rs198544702
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146668375G>T

(mRatBN7.2)4:146677093T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320325220
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146677093T>C

(mRatBN7.2)4:146677448A>T

(Rattus norvegicus)
Allele/Variant
Source: rs106777511
Genes: Emc3 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)4:146677448A>T