1,234 results
Allele/Variant Genes: Sfxn1 (Mmu)

Sfxn1em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7306013
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sfxn1em13Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7306012
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sfxn1m1Mdf

(Mus musculus)
Allele/Variant
Source: MGI:5468013
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sfxn1tm1b(EUCOMM)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:5660778
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sfxn1tm1a(EUCOMM)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:4434144
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sfxn1Gt(OST126446)Lex

(Mus musculus)
Allele/Variant
Source: MGI:4195347
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs250277376
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54225692C>T

Allele/Variant
Source: rs232705507
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54225766C>G

Allele/Variant
Source: rs250440742
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54229070A>T

Allele/Variant
Source: rs238465400
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54229155C>T

Allele/Variant
Source: rs257592979
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54229161C>G

Allele/Variant
Source: rs252447068
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54229274G>T

Allele/Variant
Source: rs244890788
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54226437C>T

Allele/Variant
Source: rs219745734
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54227020A>G

Allele/Variant
Source: rs255187885
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54227026G>A

Allele/Variant
Source: rs244768343
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54227076A>G

Allele/Variant
Source: rs47303012
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54242974G>A

Allele/Variant
Source: rs50379876
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54262292G>A

Allele/Variant
Source: rs239110887
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54247879G>C

Allele/Variant
Source: rs239104116
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54262240C>T

Allele/Variant
Source: rs263016859
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54261348A>C

Allele/Variant
Source: rs236620306
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54261663A>C

Allele/Variant
Source: rs46591199
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54260747G>A

Allele/Variant
Source: rs216918362
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54261214T>C

Allele/Variant
Source: rs49720799
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54260942G>C

Allele/Variant
Source: rs219447838
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54226834T>C

Allele/Variant
Source: rs46464325
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54247028C>G

Allele/Variant
Source: rs241986802
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54228833G>A

Allele/Variant
Source: rs263617800
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54230202C>T

Allele/Variant
Source: rs30094886
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54230647G>A

Allele/Variant
Source: rs47708589
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54230745C>T

Allele/Variant
Source: rs241256533
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54231135G>A

Allele/Variant
Source: rs248205527
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54232016C>G

Allele/Variant
Source: rs1133966630
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54232633A>G

Allele/Variant
Source: rs582937561
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54232729C>T

Allele/Variant
Source: rs51346966
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54232764A>G

Allele/Variant
Source: rs47207425
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54255014C>T

Allele/Variant
Source: rs29824928
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54255620A>G

Allele/Variant
Source: rs213509894
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54260009A>G

Allele/Variant
Source: rs240700188
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54260447A>C

Allele/Variant
Source: rs29553184
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54260636T>C

Allele/Variant
Source: rs49949689
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54260746C>T

Allele/Variant
Source: rs864289057
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54262338A>G

Allele/Variant
Source: rs586619071
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54245278C>T

Allele/Variant
Source: rs584955277
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54239619G>A

Allele/Variant
Source: rs46250077
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54246403C>T

Allele/Variant
Source: rs244440015
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54227154T>C

Allele/Variant
Source: rs266256015
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54228604G>A

Allele/Variant
Source: rs260792732
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54228848C>T

Allele/Variant
Source: rs51195589
Genes: Sfxn1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)13:54230392A>G