44 results
Allele/Variant Genes: E2f8 (Rno)

(mRatBN7.2)1:98566487C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3318986659
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98566487C>G

(mRatBN7.2)1:98580990C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318981256
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98580990C>A

(mRatBN7.2)1:98569464G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105638062
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98569464G>A

(mRatBN7.2)1:98567270A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318984551
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98567270A>T

(mRatBN7.2)1:98573950C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3318985131
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98573950C>G

(mRatBN7.2)1:98576639A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318986577
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98576639A>C

(mRatBN7.2)1:98580254T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318975327
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98580254T>C

(mRatBN7.2)1:98581483A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3318986543
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98581483A>G

(mRatBN7.2)1:98578995A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.98578995A>G
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98578995A>G

(mRatBN7.2)1:98581756G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318982480
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98581756G>A

(mRatBN7.2)1:98577367C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318983962
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98577367C>T

(mRatBN7.2)1:98583802C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318966050
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98583802C>A

(mRatBN7.2)1:98568407A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105918897
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98568407A>G

(mRatBN7.2)1:98575244T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318981175
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98575244T>C

(mRatBN7.2)1:98581685T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3318983508
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98581685T>G

(mRatBN7.2)1:98582321T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318966036
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98582321T>C

(mRatBN7.2)1:98583839C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318986186
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98583839C>T

(mRatBN7.2)1:98566292A>G

(Rattus norvegicus)
Allele/Variant
Source: rs107418748
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98566292A>G

(mRatBN7.2)1:98577902A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051336.1:g.98577902A>G
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98577902A>G

(mRatBN7.2)1:98568897T>C

(Rattus norvegicus)
Allele/Variant
Source: rs107238811
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98568897T>C

(mRatBN7.2)1:98576783T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318980140
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98576783T>C

(mRatBN7.2)1:98570166T>C

(Rattus norvegicus)
Allele/Variant
Source: rs105959080
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98570166T>C

(mRatBN7.2)1:98572212A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318977613
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98572212A>C

(mRatBN7.2)1:98574056C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318984395
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98574056C>T

(mRatBN7.2)1:98582135A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318966075
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98582135A>C

(mRatBN7.2)1:98581659G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318985740
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98581659G>A

(mRatBN7.2)1:98568600G>A

(Rattus norvegicus)
Allele/Variant
Source: rs105404346
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98568600G>A

(mRatBN7.2)1:98581755A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318986104
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98581755A>C

(mRatBN7.2)1:98569180C>T

(Rattus norvegicus)
Allele/Variant
Source: rs104902502
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98569180C>T

(mRatBN7.2)1:98568186C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318981294
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98568186C>T

(mRatBN7.2)1:98572056G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318984434
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98572056G>A

(mRatBN7.2)1:98572201A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318982484
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98572201A>T

(mRatBN7.2)1:98572834C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318986556
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98572834C>T

(mRatBN7.2)1:98576320T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318966098
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98576320T>A

(mRatBN7.2)1:98580994T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318985190
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98580994T>A

(mRatBN7.2)1:98565874C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318983654
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98565874C>T

(mRatBN7.2)1:98568496A>C

(Rattus norvegicus)
Allele/Variant
Source: rs107554233
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98568496A>C

(mRatBN7.2)1:98576461T>A

(Rattus norvegicus)
Allele/Variant
Source: rs105727457
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98576461T>A

(mRatBN7.2)1:98581736G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318983984
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98581736G>C

(mRatBN7.2)1:98581178T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318981140
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98581178T>C

(mRatBN7.2)1:98584101T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3318984490
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98584101T>C

(mRatBN7.2)1:98565817G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318977632
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98565817G>A

(mRatBN7.2)1:98570674C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3318977607
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98570674C>A

(mRatBN7.2)1:98572496C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3318975337
Genes: E2f8 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:98572496C>T