98 results
Allele/Variant Genes: E2f2 (Rno)

(mRatBN7.2)5:148409783A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320616982
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148409783A>T

(mRatBN7.2)5:148410565G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323735943
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148410565G>T

(mRatBN7.2)5:148408086T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320743676
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148408086T>C

(mRatBN7.2)5:148410364T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051340.1:g.148410364T>C
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148410364T>C

(mRatBN7.2)5:148411689C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320617032
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148411689C>T

(mRatBN7.2)5:148418647G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320676816
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148418647G>T

(mRatBN7.2)5:148402235C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320693016
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148402235C>T

(mRatBN7.2)5:148404228T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320706518
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148404228T>C

(mRatBN7.2)5:148407429G>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320616984
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148407429G>C

(mRatBN7.2)5:148407745T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320637781
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148407745T>C

(mRatBN7.2)5:148403151A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320690512
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148403151A>G

(mRatBN7.2)5:148418226G>T

(Rattus norvegicus)
Allele/Variant
Source: rs197972064
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148418226G>T

(mRatBN7.2)5:148401969A>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320706532
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148401969A>T

(mRatBN7.2)5:148402704A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320743625
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148402704A>C

(mRatBN7.2)5:148403411A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320647383
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148403411A>C

(mRatBN7.2)5:148404099T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320723284
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148404099T>C

(mRatBN7.2)5:148404321C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320703598
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148404321C>T

(mRatBN7.2)5:148406906C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320676752
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148406906C>T

(mRatBN7.2)5:148410041C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320743642
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148410041C>A

(mRatBN7.2)5:148410287T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320637873
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148410287T>C

(mRatBN7.2)5:148416879T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320690556
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148416879T>G

(mRatBN7.2)5:148417906T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320728622
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148417906T>A

(mRatBN7.2)5:148416905G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320647415
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148416905G>A

(mRatBN7.2)5:148404227T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320703587
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148404227T>G

(mRatBN7.2)5:148407350A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320706497
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148407350A>G

(mRatBN7.2)5:148402703C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320706448
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148402703C>A

(mRatBN7.2)5:148422263G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320637786
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148422263G>T

(mRatBN7.2)5:148422371G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320690564
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148422371G>A

(mRatBN7.2)5:148410777T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320547611
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148410777T>C

(mRatBN7.2)5:148413376C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320637767
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148413376C>T

(mRatBN7.2)5:148402883T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320706524
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148402883T>C

(mRatBN7.2)5:148416661C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320706457
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148416661C>T

(mRatBN7.2)5:148416837A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051340.1:g.148416837A>G
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148416837A>G

(mRatBN7.2)5:148417452G>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051340.1:g.148417452G>A
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148417452G>A

(mRatBN7.2)5:148407336T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320547762
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148407336T>G

(mRatBN7.2)5:148403228C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320719212
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148403228C>T

(mRatBN7.2)5:148403955A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320723199
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148403955A>G

(mRatBN7.2)5:148404593T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320547752
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148404593T>A

(mRatBN7.2)5:148410032C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320647388
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148410032C>T

(mRatBN7.2)5:148418066T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320743492
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148418066T>C

(mRatBN7.2)5:148422245T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320703543
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148422245T>G

(mRatBN7.2)5:148419134A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320692917
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148419134A>G

(mRatBN7.2)5:148419728C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320676819
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148419728C>T

(mRatBN7.2)5:148420557A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320690524
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148420557A>G

(mRatBN7.2)5:148422268C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320676728
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148422268C>T

(mRatBN7.2)5:148422480G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320743667
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148422480G>T

(mRatBN7.2)5:148414268C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320676853
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148414268C>A

(mRatBN7.2)5:148415734C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320676803
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148415734C>T

(mRatBN7.2)5:148415818C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320690485
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148415818C>T

(mRatBN7.2)5:148417275C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320692781
Genes: E2f2 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)5:148417275C>T