1,757 results
Allele/Variant Genes: Btbd7 (Mmu)

Btbd7tm1Kmy

(Mus musculus)
Allele/Variant
Source: MGI:5908734
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Btbd7em1(IMPC)Ccpcz

(Mus musculus)
Allele/Variant
Source: MGI:6385277
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Btbd7tm1.1Kmy

(Mus musculus)
Allele/Variant
Source: MGI:6259681
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs579974163
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102751615C>T

Allele/Variant
Source: rs585586782
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102749064A>T

Allele/Variant
Source: rs238426614
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102754208G>A

Allele/Variant
Source: rs107911296
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102750321C>A

Allele/Variant
Source: rs582332412
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102752488A>G

Allele/Variant
Source: rs585065166
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102752875G>T

Allele/Variant
Source: rs580854706
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102753784A>G

Allele/Variant
Source: rs108738145
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102750878A>T

Allele/Variant
Source: rs230127768
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102757505G>A

Allele/Variant
Source: rs257913948
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102754947G>A

Allele/Variant
Source: rs252716056
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102766910T>C

Allele/Variant
Source: rs215114527
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102772948C>T

Allele/Variant
Source: rs226167499
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102748908G>A

Allele/Variant
Source: rs249947754
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102754790C>T

Allele/Variant
Source: rs586925822
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102755348T>C

Allele/Variant
Source: rs256283328
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102755670A>G

Allele/Variant
Source: rs49207591
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102753112C>T

Allele/Variant
Source: rs213121922
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102756860C>T

Allele/Variant
Source: rs249075302
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102757523C>T

Allele/Variant
Source: rs222855469
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102756149G>A

Allele/Variant
Source: rs584112015
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102751697A>G

Allele/Variant
Source: rs218890328
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102752199A>G

Allele/Variant
Source: rs581794685
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102748206A>G

Allele/Variant
Source: rs256074631
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102749073C>T

Allele/Variant
Source: rs586022163
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102750035A>G

Allele/Variant
Source: rs1132056900
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102750383C>T

Allele/Variant
Source: rs262328640
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102763977C>T

Allele/Variant
Source: rs265336741
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102764415T>C

Allele/Variant
Source: rs216959006
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102759321A>T

Allele/Variant
Source: rs218133012
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102759471A>G

Allele/Variant
Source: rs256388185
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102751570T>C

Allele/Variant
Source: rs581140508
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102751751C>T

Allele/Variant
Source: rs217972572
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102748155A>C

Allele/Variant
Source: rs579267183
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102749225C>T

Allele/Variant
Source: rs1134981610
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102750336T>G

Allele/Variant
Source: rs583450451
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102752831A>T

Allele/Variant
Source: rs212859229
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102753248T>C

Allele/Variant
Source: rs46475384
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102753268T>A

Allele/Variant
Source: rs583458801
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102753300C>T

Allele/Variant
Source: rs579072888
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102754165C>G

Allele/Variant
Source: rs239892851
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102764568A>G

Allele/Variant
Source: rs225121173
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102747699G>A

Allele/Variant
Source: rs235743961
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102760242C>T

Allele/Variant
Source: rs582546079
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102760306C>T

Allele/Variant
Source: rs211960970
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102760392A>C

Allele/Variant
Source: rs234860191
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102762860T>G

Allele/Variant
Source: rs584742971
Genes: Btbd7 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:102763508C>T