805 results
Allele/Variant Genes: Ube2d1 (Mmu)
Allele/Variant
Source: MGI:6324191
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: MGI:5527597
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs229949713
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71091140C>T

Allele/Variant
Source: rs238740857
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71092009C>A

Allele/Variant
Source: rs262555397
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71092252C>A

Allele/Variant
Source: rs221762941
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71092336A>G

Allele/Variant
Source: rs256296878
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71092711T>C

Allele/Variant
Source: rs265066597
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71093734C>T

Allele/Variant
Source: rs222815946
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71097287A>G

Allele/Variant
Source: rs257634122
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71097349G>C

Allele/Variant
Source: rs214423885
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71099049T>A

Allele/Variant
Source: rs233705535
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71099051C>T

Allele/Variant
Source: rs1134806693
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71091543A>T

Allele/Variant
Source: rs247272136
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71092139T>G

Allele/Variant
Source: rs257509580
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71099217G>A

Allele/Variant
Source: rs239294821
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71101208T>A

Allele/Variant
Source: rs220289193
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71101293T>C

Allele/Variant
Source: rs29940385
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71101476T>C

Allele/Variant
Source: rs231171260
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71101639G>A

Allele/Variant
Source: rs580746030
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71101690C>A

Allele/Variant
Source: rs29940391
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71102050G>T

Allele/Variant
Source: rs260089624
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71102714A>G

Allele/Variant
Source: rs229101797
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71098875G>A

Allele/Variant
Source: rs251377371
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71099106A>T

Allele/Variant
Source: rs29939565
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71099706C>G

Allele/Variant
Source: rs256522474
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71099775C>G

Allele/Variant
Source: rs583913277
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71101692C>T

Allele/Variant
Source: rs244535369
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71103807T>C

Allele/Variant
Source: rs214389981
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71104631T>C

Allele/Variant
Source: rs263850411
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71104930T>G

Allele/Variant
Source: rs251570852
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71105992C>T

Allele/Variant
Source: rs259912977
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71106181G>A

Allele/Variant
Source: rs29941313
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71091374C>T

Allele/Variant
Source: rs241077623
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71091566G>A

Allele/Variant
Source: rs29942215
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71091575G>A

Allele/Variant
Source: rs214318131
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71092001T>A

Allele/Variant
Source: rs583009649
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71092308C>T

Allele/Variant
Source: rs234500342
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71093082C>T

Allele/Variant
Source: rs265354256
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71097278G>A

Allele/Variant
Source: rs234738222
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71098378C>T

Allele/Variant
Source: rs1132207418
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71098530G>T

Allele/Variant
Source: rs258997268
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71098704G>A

Allele/Variant
Source: rs241100513
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71099282C>A

Allele/Variant
Source: rs258875659
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71099291C>T

Allele/Variant
Source: rs260058946
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71100598C>T

Allele/Variant
Source: rs225879057
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71102009G>A

Allele/Variant
Source: rs259977932
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71103061C>T

Allele/Variant
Source: rs239200914
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71102150C>T

Allele/Variant
Source: rs232822118
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71102265G>C

Allele/Variant
Source: rs215848348
Genes: Ube2d1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm38)10:71102374A>G