516 results
Allele/Variant Genes: Sod2 (Mmu)

Sod2tm1Shs

(Mus musculus)
Allele/Variant
Source: MGI:2447406
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: congestive heart failure, dilated cardiomyopathy
Variant Name: Not Available

Sod2tm1Cje

(Mus musculus)
Allele/Variant
Source: MGI:1857344
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Canavan disease, Leigh disease, amyotrophic lateral sclerosis type 1
Variant Name: Not Available

Allele/Variant
Source: MGI:4818481
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sod2em1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7292520
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sod2em18Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7306609
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sod2em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7306610
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sod2tm1Smel

(Mus musculus)
Allele/Variant
Source: MGI:5788667
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sod2tm1.1Mrl

(Mus musculus)
Allele/Variant
Source: MGI:6434806
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sod2em2Cya

(Mus musculus)
Allele/Variant
Source: MGI:7586760
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sod2em1Cya

(Mus musculus)
Allele/Variant
Source: MGI:7586759
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sod2tm1Kskk

(Mus musculus)
Allele/Variant
Source: MGI:5774733
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sod2tm1Leb

(Mus musculus)
Allele/Variant
Source: MGI:1857480
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: MGI:5568594
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Sod2tm1.1Kskk

(Mus musculus)
Allele/Variant
Source: MGI:3578627
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs584155691
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13231865A>C

Allele/Variant
Source: rs48502437
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13241539A>T

Allele/Variant
Source: rs47593554
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13241557A>T

Allele/Variant
Source: rs47864853
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13242085C>A

Allele/Variant
Source: rs583144786
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13242686T>A

Allele/Variant
Source: rs216714540
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13236089C>A

Allele/Variant
Source: rs51957079
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13243001T>G

Allele/Variant
Source: rs586994694
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13243755T>G

Allele/Variant
Source: rs585347302
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13236341T>C

Allele/Variant
Source: rs579123078
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13244147C>T

Allele/Variant
Source: rs46978037
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13247435G>T

Allele/Variant
Source: rs51765973
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13249871A>G

Allele/Variant
Source: rs581379513
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13248964A>C

Allele/Variant
Source: rs583307933
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13250724A>C

Allele/Variant
Source: rs49797632
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13256625T>C

Allele/Variant
Source: rs1133369323
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13257509C>T

Allele/Variant
Source: rs214223880
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13226317C>T

Allele/Variant
Source: rs1133661884
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13230084T>G

Allele/Variant
Source: rs108465503
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13230225T>A

Allele/Variant
Source: rs245215611
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13230343G>C

Allele/Variant
Source: rs580232543
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13247128G>T

Allele/Variant
Source: rs578759986
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13248989C>T

Allele/Variant
Source: rs586926279
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13251055C>A

Allele/Variant
Source: rs585194953
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13251279C>T

Allele/Variant
Source: rs580684573
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13253054A>C

Allele/Variant
Source: rs586593384
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13255206G>A

Allele/Variant
Source: rs582290974
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13256552G>A

Allele/Variant
Source: rs1132375365
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13256566A>T

Allele/Variant
Source: rs586482746
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13256976T>A

Allele/Variant
Source: rs263028546
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13226472G>T

Allele/Variant
Source: rs48506918
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13251146C>T

Allele/Variant
Source: rs49202389
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13251205G>T

Allele/Variant
Source: rs49913466
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13251276A>T

Allele/Variant
Source: rs584464941
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13252819C>A

Allele/Variant
Source: rs578587390
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13252832C>T

Allele/Variant
Source: rs1134420838
Genes: Sod2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:13253995C>A