89 results
Allele/Variant Genes: Smg7 (Rno)

(mRatBN7.2)13:65002082T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322338253
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65002082T>A

(mRatBN7.2)13:65013280C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197475922
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65013280C>T

(mRatBN7.2)13:65026927A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051348.1:g.65026927A>G
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65026927A>G

(mRatBN7.2)13:65035296C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322058630
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65035296C>T

(mRatBN7.2)13:64987396G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198986982
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64987396G>A

(mRatBN7.2)13:65049739C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322058550
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65049739C>T

(mRatBN7.2)13:65010868C>G

(Rattus norvegicus)
Allele/Variant
Source: rs105363347
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65010868C>G

(mRatBN7.2)13:65023642C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322374291
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65023642C>T

(mRatBN7.2)13:65031222C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322400320
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65031222C>T

(mRatBN7.2)13:64988179T>C

(Rattus norvegicus)
Allele/Variant
Source: rs197113221
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64988179T>C

(mRatBN7.2)13:65035181A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322436689
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65035181A>G

(mRatBN7.2)13:64987777C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051348.1:g.64987777C>T
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64987777C>T

(mRatBN7.2)13:64988616C>T

(Rattus norvegicus)
Allele/Variant
Source: rs8163461
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64988616C>T

(mRatBN7.2)13:64997879C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322427817
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64997879C>A

(mRatBN7.2)13:65000028C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322436696
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65000028C>T

(mRatBN7.2)13:65008065T>C

(Rattus norvegicus)
Allele/Variant
Source: rs198900509
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65008065T>C

(mRatBN7.2)13:65023172G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322227137
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65023172G>A

(mRatBN7.2)13:65024811C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322377773
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65024811C>T

(mRatBN7.2)13:65029792G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322371859
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65029792G>C

(mRatBN7.2)13:65032257A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322377869
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65032257A>G

(mRatBN7.2)13:64995831C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105351568
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64995831C>T

(mRatBN7.2)13:65045868G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322374408
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65045868G>A

(mRatBN7.2)13:64997292G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322264694
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64997292G>A

(mRatBN7.2)13:65013705C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322377890
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65013705C>T

(mRatBN7.2)13:65020126A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322371866
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65020126A>G

(mRatBN7.2)13:65033402A>G

(Rattus norvegicus)
Allele/Variant
Source: rs106588610
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65033402A>G

(mRatBN7.2)13:65036194A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322394269
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65036194A>G

(mRatBN7.2)13:64986156T>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051348.1:g.64986156T>G
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64986156T>G

(mRatBN7.2)13:64986984C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322374218
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64986984C>T

(mRatBN7.2)13:65040258A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322425571
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65040258A>G

(mRatBN7.2)13:64997968C>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051348.1:g.64997968C>A
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64997968C>A

(mRatBN7.2)13:65016052A>G

(Rattus norvegicus)
Allele/Variant
Source: rs107583558
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65016052A>G

(mRatBN7.2)13:65023640C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322374401
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65023640C>T

(mRatBN7.2)13:65040155G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322425615
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65040155G>A

(mRatBN7.2)13:64989364C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322420800
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64989364C>T

(mRatBN7.2)13:64992821G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322338260
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64992821G>A

(mRatBN7.2)13:64994881G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322374343
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64994881G>A

(mRatBN7.2)13:64995479A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322338307
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64995479A>G

(mRatBN7.2)13:64996660G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198405428
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64996660G>A

(mRatBN7.2)13:65006030T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322425604
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65006030T>C

(mRatBN7.2)13:64990810T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3322400529
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64990810T>A

(mRatBN7.2)13:64995692G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3322058594
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:64995692G>C

(mRatBN7.2)13:65004025C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322371800
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65004025C>T

(mRatBN7.2)13:65004647T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106144971
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65004647T>C

(mRatBN7.2)13:65026995A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322058584
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65026995A>G

rs198192840

(Rattus norvegicus)
Allele/Variant
Source: rs198192840
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: Not Available

(mRatBN7.2)13:65034934C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3322264716
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65034934C>T

(mRatBN7.2)13:65035543T>C

(Rattus norvegicus)
Allele/Variant
Source: rs197059079
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65035543T>C

(mRatBN7.2)13:65038626A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3322227165
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65038626A>G

(mRatBN7.2)13:65049713C>T

(Rattus norvegicus)
Allele/Variant
Source: rs106236993
Genes: Smg7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)13:65049713C>T