715 results
Allele/Variant Genes: E2f2 (Mmu)

E2f2em1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7289428
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

E2f2em3Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7298312
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

E2f2tm1Zubi

(Mus musculus)
Allele/Variant
Source: MGI:2179111
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

E2f2em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7298311
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs32321209
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135903517C>T

Allele/Variant
Source: rs3697251
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135901720A>G

Allele/Variant
Source: rs229051337
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135902906C>T

Allele/Variant
Source: rs27580018
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135904440T>C

Allele/Variant
Source: rs241892916
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135904457G>A

Allele/Variant
Source: rs3698546
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135901974G>A

Allele/Variant
Source: rs586056235
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135905664A>T

Allele/Variant
Source: rs27580009
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135906805T>A

Allele/Variant
Source: rs251715822
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135909210T>C

Allele/Variant
Source: rs217988570
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135915253C>A

Allele/Variant
Source: rs27580026
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135903367G>A

Allele/Variant
Source: rs265966208
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135900531C>G

Allele/Variant
Source: rs216441893
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135901023G>C

Allele/Variant
Source: rs3659740
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135903006A>G

Allele/Variant
Source: rs252391770
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135903297A>G

Allele/Variant
Source: rs864278668
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135901733T>C

Allele/Variant
Source: rs262349743
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135904640A>G

Allele/Variant
Source: rs32884275
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135904846T>C

Allele/Variant
Source: rs255770424
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135905342C>T

Allele/Variant
Source: rs1135148023
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135905662G>C

Allele/Variant
Source: rs27580021
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135903785G>A

Allele/Variant
Source: rs215914919
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135901224G>A

Allele/Variant
Source: rs3697264
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135901726T>C

Allele/Variant
Source: rs252852692
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135904042G>A

Allele/Variant
Source: rs215183679
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135905343A>G

Allele/Variant
Source: rs587003252
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135906295T>C

Allele/Variant
Source: rs235142748
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135908159C>A

Allele/Variant
Source: rs258081461
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135908257C>T

Allele/Variant
Source: rs253230405
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135910816T>C

Allele/Variant
Source: rs587395372
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135911169C>T

Allele/Variant
Source: rs227473071
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135903619C>T

Allele/Variant
Source: rs32078934
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135902907T>G

Allele/Variant
Source: rs246566440
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135904068C>T

Allele/Variant
Source: rs227280378
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135904216T>C

Allele/Variant
Source: rs215552970
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135904402C>T

Allele/Variant
Source: rs258138869
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135904487G>A

Allele/Variant
Source: rs244554242
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135901728T>A

Allele/Variant
Source: rs50874498
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135906057G>A

Allele/Variant
Source: rs46830718
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135906072C>T

Allele/Variant
Source: rs214965511
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135906290C>T

Allele/Variant
Source: rs257261323
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135915993T>C

Allele/Variant
Source: rs212259764
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135916160G>A

Allele/Variant
Source: rs250283279
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135918848C>T

Allele/Variant
Source: rs50536320
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135920102A>G

Allele/Variant
Source: rs229495248
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135900589C>T

Allele/Variant
Source: rs220550262
Genes: E2f2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)4:135901415G>C