106 results
Allele/Variant Genes: Prph (Mmu)

Prphem1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7304814
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Prphtm1Jpj

(Mus musculus)
Allele/Variant
Source: MGI:2180052
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Prphem3Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7304815
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs239731801
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98955535C>T

Allele/Variant
Source: rs255540388
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98954457G>C

Allele/Variant
Source: rs256236480
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952686T>C

Allele/Variant
Source: rs225270537
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952701T>A

Allele/Variant
Source: rs1134343837
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98955634G>A

Allele/Variant
Source: rs220670444
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98956058C>T

Allele/Variant
Source: rs259123600
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98954733G>C

Allele/Variant
Source: rs213376180
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98954925G>A

Allele/Variant
Source: rs32444457
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98951521A>T

Allele/Variant
Source: rs250265194
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98951602C>T

Allele/Variant
Source: rs245430475
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98954859G>A

Allele/Variant
Source: rs229626095
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98953339C>T

Allele/Variant
Source: rs219825743
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98951469T>C

Allele/Variant
Source: rs245875285
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952129C>T

Allele/Variant
Source: rs240130314
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952245A>G

Allele/Variant
Source: rs258831978
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952252C>T

Allele/Variant
Source: rs1134488571
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952265G>A

Allele/Variant
Source: rs1132540747
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952271T>C

Allele/Variant
Source: rs252378346
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952275A>C

Allele/Variant
Source: rs242447131
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98953689C>A

Allele/Variant
Source: rs31943680
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98953936G>A

Allele/Variant
Source: rs32176664
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98955816G>A

Allele/Variant
Source: rs238399280
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98954386C>A

Allele/Variant
Source: rs215831281
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952176C>T

Allele/Variant
Source: rs235020614
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952277G>C

Allele/Variant
Source: rs241529489
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98951512G>A

Allele/Variant
Source: rs46065416
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952006G>A

Allele/Variant
Source: rs32092478
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98951678G>A

Allele/Variant
Source: rs1134786585
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952264G>T

Allele/Variant
Source: rs219899221
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952276G>C

Allele/Variant
Source: rs238458662
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952559G>T

Allele/Variant
Source: rs258083389
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952880T>C

Allele/Variant
Source: rs32261265
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952990G>C

Allele/Variant
Source: rs239514781
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98956277T>G

Allele/Variant
Source: rs232056326
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98956294T>A

Allele/Variant
Source: rs1133396370
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952317A>G

Allele/Variant
Source: rs246432067
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98954545C>A

Allele/Variant
Source: rs48080946
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98955758T>C

Allele/Variant
Source: rs227073039
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98953681T>C

Allele/Variant
Source: rs1134003759
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98956081T>A

Allele/Variant
Source: rs1132383612
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98952268A>T

Allele/Variant
Source: rs234534156
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98956440G>A

Allele/Variant
Source: rs216106593
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98956698C>A

Allele/Variant
Source: rs226671942
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98956767A>G

Allele/Variant
Source: rs233714164
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98954676A>G

Allele/Variant
Source: rs224014998
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98954799G>A

Allele/Variant
Source: rs211861081
Genes: Prph (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:98954529G>T