45 results
Allele/Variant Genes: Slmap (Mmu) Molecular Consequence: intron variant

Slmapem2Cya

(Mus musculus)
Allele/Variant
Source: MGI:7586688
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Slmapem1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7306484
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: MGI:5287507
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Slmapem1Cya

(Mus musculus)
Allele/Variant
Source: MGI:7586687
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Slmaptm1.2Tuab

(Mus musculus)
Allele/Variant
Source: MGI:7780106
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Slmaptm1.1Tuab

(Mus musculus)
Allele/Variant
Source: MGI:7704162
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Slmapem1(IMPC)J

(Mus musculus)
Allele/Variant
Source: MGI:5812880
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs242960570
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26134860C>T

Allele/Variant
Source: rs38073031
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26135108T>A

Allele/Variant
Source: rs47469524
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26135676A>C

Allele/Variant
Source: rs256663914
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26148455C>T

Allele/Variant
Source: rs36321808
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26134741G>C

Allele/Variant
Source: rs245896755
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26134814C>T

Allele/Variant
Source: rs230517057
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26135472T>C

Allele/Variant
Source: rs246286908
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26135993G>A

Allele/Variant
Source: rs37807204
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26134791A>G

Allele/Variant
Source: rs221071876
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26134845C>T

Allele/Variant
Source: rs260770739
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26135082C>T

Allele/Variant
Source: rs13464020
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26135219G>A

Allele/Variant
Source: rs37036610
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26149428T>C

Allele/Variant
Source: rs219279237
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26254863C>T

Allele/Variant
Source: rs236878976
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26148586T>C

Allele/Variant
Source: rs251610378
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26148685G>A

Allele/Variant
Source: rs249377034
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26135449C>T

Allele/Variant
Source: rs36574093
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26143629G>A

Allele/Variant
Source: rs246302218
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26160106T>G

Allele/Variant
Source: rs36260076
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26183461A>G

Allele/Variant
Source: rs37047758
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26139319C>T

Allele/Variant
Source: rs253878923
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26147794C>A

Allele/Variant
Source: rs36855187
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26183482C>T

Allele/Variant
Source: rs263751228
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26160116G>A

Allele/Variant
Source: rs249259913
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26255230G>C

Allele/Variant
Source: rs260010881
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26134842G>C

Allele/Variant
Source: rs224698436
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26160161T>G

Allele/Variant
Source: rs218307474
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26255360G>C

Allele/Variant
Source: rs235350184
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26134702T>C

Allele/Variant
Source: rs218607968
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26148564C>T

Allele/Variant
Source: rs36932859
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26134716C>T

Allele/Variant
Source: rs265350011
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26135470T>C

Allele/Variant
Source: rs258353756
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26143720C>T

Allele/Variant
Source: rs36596275
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26135293T>C

Allele/Variant
Source: rs232342620
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26255397C>G

Allele/Variant
Source: rs39547035
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26204014G>A

Allele/Variant
Source: rs1133878096
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26255695G>C

Allele/Variant
Source: rs234465481
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26254892A>T