3,058 results
Allele/Variant Genes: Slmap (Mmu)

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: rs36740679
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26145485A>G

Allele/Variant
Source: rs37166974
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26145843C>T

Allele/Variant
Source: rs212764695
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26179959C>T

Allele/Variant
Source: rs37121215
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26180305T>A

Allele/Variant
Source: rs212277564
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26182595C>T

Allele/Variant
Source: rs37541816
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26182247T>G

Allele/Variant
Source: rs222505508
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26191864G>C

Allele/Variant
Source: rs240614885
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26191867T>A

Allele/Variant
Source: rs36364938
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26193838G>A

Allele/Variant
Source: rs240438030
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26192439A>T

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: rs579582533
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26136965G>A

Allele/Variant
Source: rs51292448
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26145514C>T

Allele/Variant
Source: rs221297191
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26146102G>A

Allele/Variant
Source: rs37119007
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26147259A>C

Allele/Variant
Source: rs36831738
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26147467G>C

Allele/Variant
Source: rs1133494834
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26147540G>A

Allele/Variant
Source: rs37474603
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26203105T>C

Allele/Variant
Source: rs233184846
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26203143A>G

Allele/Variant
Source: rs250152645
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26210730T>C

Allele/Variant
Source: rs585881625
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26210919T>C

Allele/Variant
Source: rs226419989
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26210974C>T

Allele/Variant
Source: rs241982152
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26211014T>C

Allele/Variant
Source: rs579765347
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26208369A>G

Allele/Variant
Source: rs586695419
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26208591T>A

Allele/Variant
Source: rs235043423
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26208911A>G

Allele/Variant
Source: rs263627482
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26208971C>T

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: rs217695830
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26136600G>A

Allele/Variant
Source: rs236313653
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26138659T>C

Allele/Variant
Source: rs247988200
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26139966C>T

Allele/Variant
Source: rs244207115
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26137634T>C

Allele/Variant
Source: rs1133726181
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26140389C>T

Allele/Variant
Source: rs36900886
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26138197C>A

Allele/Variant
Source: rs1132224883
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26138404G>T

Allele/Variant
Source: rs217442839
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26141256G>A

Allele/Variant
Source: rs211706569
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26143824G>A

Allele/Variant
Source: rs220831901
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26197094T>A

Allele/Variant
Source: rs238727029
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26195459A>G

Allele/Variant
Source: rs231036705
Genes: Slmap (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)14:26193974T>A