1,411 results
Allele/Variant Genes: E2f7 (Mmu)

E2f7em2Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7376495
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

E2f7tm1a(KOMP)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:4363426
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

E2f7tm1Gle

(Mus musculus)
Allele/Variant
Source: MGI:3773721
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

E2f7tm1.1Gle

(Mus musculus)
Allele/Variant
Source: MGI:3773722
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

E2f7em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7376494
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

E2f7tm1b(KOMP)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:5471144
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs29344175
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110580865T>C

Allele/Variant
Source: rs583915377
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110581963T>G

Allele/Variant
Source: rs29377841
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110582008C>T

Allele/Variant
Source: rs226181902
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110582356A>T

Allele/Variant
Source: rs245389080
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110582378T>A

Allele/Variant
Source: rs29322440
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110582828T>G

Allele/Variant
Source: rs215341756
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110582911G>A

Allele/Variant
Source: rs249127397
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110583278G>A

Allele/Variant
Source: rs248538022
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110583615A>G

Allele/Variant
Source: rs240645044
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110584650A>G

Allele/Variant
Source: rs234412435
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110581221G>C

Allele/Variant
Source: rs29349036
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110583163G>A

Allele/Variant
Source: rs237022479
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110584080G>A

Allele/Variant
Source: rs262940966
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110583358T>C

Allele/Variant
Source: rs579625139
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110584170C>G

Allele/Variant
Source: rs263826935
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110583638G>A

Allele/Variant
Source: rs221659025
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110583688C>T

Allele/Variant
Source: rs30817970
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110587834G>A

Allele/Variant
Source: rs30818882
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110589280T>C

Allele/Variant
Source: rs236880946
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110589540A>C

Allele/Variant
Source: rs29334890
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110581693C>T

Allele/Variant
Source: rs220287433
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110583027G>T

Allele/Variant
Source: rs225687880
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110583304G>T

Allele/Variant
Source: rs51069844
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110584576G>A

Allele/Variant
Source: rs30818874
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110588278T>C

Allele/Variant
Source: rs48153989
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110588566G>A

Allele/Variant
Source: rs240103912
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110588844G>A

Allele/Variant
Source: rs266196652
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110588948C>T

Allele/Variant
Source: rs30812963
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110590259G>A

Allele/Variant
Source: rs238746437
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110592128C>T

Allele/Variant
Source: rs249154715
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110581851C>T

Allele/Variant
Source: rs237774694
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110582472G>A

Allele/Variant
Source: rs254767847
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110582541A>C

Allele/Variant
Source: rs228695733
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110582589A>T

Allele/Variant
Source: rs224504360
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110583571T>C

Allele/Variant
Source: rs242611548
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110590272T>C

Allele/Variant
Source: rs230994624
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110590289G>A

Allele/Variant
Source: rs251397223
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110590465A>G

Allele/Variant
Source: rs30815954
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110591608A>T

Allele/Variant
Source: rs49673001
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110591236C>T

Allele/Variant
Source: rs30817968
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110587753C>G

Allele/Variant
Source: rs107753182
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110588071A>G

Allele/Variant
Source: rs245628920
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110588924G>T

Allele/Variant
Source: rs30818880
Genes: E2f7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:110589250T>C