1,361 results
Allele/Variant Genes: Scyl2 (Mmu)

Scyl2tm1.2Spel

(Mus musculus)
Allele/Variant
Source: MGI:5752502
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Scyl2tm1.1Spel

(Mus musculus)
Allele/Variant
Source: MGI:5752500
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs246669624
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89492612C>T

Allele/Variant
Source: rs13474658
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89475085C>T

Allele/Variant
Source: rs1133925640
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89475669G>T

Allele/Variant
Source: rs261022713
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89481628G>C

Allele/Variant
Source: rs224666613
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89481190T>C

Allele/Variant
Source: rs241343783
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89482464C>A

Allele/Variant
Source: rs578497004
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89483056C>A

Allele/Variant
Source: rs256997750
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89483462T>C

Allele/Variant
Source: rs51993578
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89484125T>G

Allele/Variant
Source: rs30332416
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89484365A>G

Allele/Variant
Source: rs29343422
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89474640C>T

Allele/Variant
Source: rs232031569
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89474645T>C

Allele/Variant
Source: rs213858899
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89474755C>T

Allele/Variant
Source: rs237343848
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89475034T>C

Allele/Variant
Source: rs52479503
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89475174T>C

Allele/Variant
Source: rs30332157
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89475269T>C

Allele/Variant
Source: rs29349665
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89484022T>A

Allele/Variant
Source: rs587062660
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89484097T>C

Allele/Variant
Source: rs247708860
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89485430C>T

Allele/Variant
Source: rs255830950
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89485665A>G

Allele/Variant
Source: rs30332163
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89475629C>T

Allele/Variant
Source: rs29344052
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89482641G>A

Allele/Variant
Source: rs243676211
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89482821G>A

Allele/Variant
Source: rs583296945
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89484089G>A

Allele/Variant
Source: rs234068850
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89484764T>G

Allele/Variant
Source: rs213957389
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89484819T>G

Allele/Variant
Source: rs231151996
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89484843C>T

Allele/Variant
Source: rs30332420
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89484860A>C

Allele/Variant
Source: rs30332422
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89484955C>T

Allele/Variant
Source: rs235584649
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89484172A>G

Allele/Variant
Source: rs30332155
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89475028A>T

Allele/Variant
Source: rs262848993
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89475190T>C

Allele/Variant
Source: rs579579000
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89475859C>T

Allele/Variant
Source: rs29333759
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89475887A>G

Allele/Variant
Source: rs219652056
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89476796G>A

Allele/Variant
Source: rs239936541
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89477635C>T

Allele/Variant
Source: rs30335378
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89478256T>C

Allele/Variant
Source: rs219491834
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89478602C>T

Allele/Variant
Source: rs29376927
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89478915G>T

Allele/Variant
Source: rs29318290
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89479554G>A

Allele/Variant
Source: rs30334164
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89486021A>G

Allele/Variant
Source: rs233777748
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89486118T>C

Allele/Variant
Source: rs51901619
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89497840T>C

Allele/Variant
Source: rs29335108
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89499544T>C

Allele/Variant
Source: rs50893372
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89506399C>T

Allele/Variant
Source: rs30334050
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89506499A>G

Allele/Variant
Source: rs30336004
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89506950A>C

Allele/Variant
Source: rs233389204
Genes: Scyl2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:89508751G>A