18 results
Allele/Variant Genes: Traf3ip3 (Mmu) Molecular Consequence: missense variant
Allele/Variant
Source: rs33131431
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192860530T>A

Allele/Variant
Source: rs250528166
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192877660C>T

Allele/Variant
Source: rs13499787
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192864252G>A

Allele/Variant
Source: rs240106048
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192867082G>A

Allele/Variant
Source: rs244980986
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192868984C>T

Allele/Variant
Source: rs13499755
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192880036G>A

Allele/Variant
Source: rs217789651
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192867052G>T

Allele/Variant
Source: rs13491012
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192880081C>T

Allele/Variant
Source: rs224815631
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192877155C>T

Allele/Variant
Source: rs220708108
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192864226C>G

Allele/Variant
Source: rs13491020
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192876681A>T

Allele/Variant
Source: rs13491089
Genes: A130010J15Rik (Mmu), Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192858057C>T

Allele/Variant
Source: rs13499758
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192877702G>T

Allele/Variant
Source: rs226353774
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192864286G>T

Allele/Variant
Source: rs13491090
Genes: A130010J15Rik (Mmu), Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192857989T>A

Allele/Variant
Source: rs237116301
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192877634C>T

Allele/Variant
Source: rs13491017
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192877157T>G

Allele/Variant
Source: rs251051252
Genes: Traf3ip3 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)1:192867089A>G