Product Details

SNP ID
rs61192205
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:30721465 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CGCGGGATGGGCGCGCGGCTGGTGC[C/T]TGGGCTGCTGCCTCCTCCTGCCGCT
Phenotype
MIM: 602988
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
PCDH7 PubMed Links

Gene Details

Gene
PCDH7
Gene Name
protocadherin 7
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001173523.1 1087 Silent Mutation CTG,TTG L15L NP_001166994.1
NM_002589.2 1087 Silent Mutation CTG,TTG L15L NP_002580.2
NM_032456.2 1087 Silent Mutation CTG,TTG L15L NP_115832.1
NM_032457.3 1087 Silent Mutation CTG,TTG L15L NP_115833.2
XM_005248163.3 1087 Silent Mutation CTG,TTG L15L XP_005248220.1
XM_005248164.3 1087 Silent Mutation CTG,TTG L15L XP_005248221.1
XM_005248166.3 1087 Silent Mutation CTG,TTG L15L XP_005248223.1
XM_011513842.2 1087 Silent Mutation CTG,TTG L15L XP_011512144.1
XM_011513843.2 1087 Silent Mutation CTG,TTG L15L XP_011512145.1
XM_011513844.2 1087 Silent Mutation CTG,TTG L15L XP_011512146.1
XM_017008259.1 1087 Silent Mutation CTG,TTG L15L XP_016863748.1
XM_017008260.1 1087 Silent Mutation CTG,TTG L15L XP_016863749.1
XM_017008261.1 1087 Silent Mutation CTG,TTG L15L XP_016863750.1
XM_017008262.1 1087 Silent Mutation CTG,TTG L15L XP_016863751.1
XM_017008263.1 1087 Silent Mutation CTG,TTG L15L XP_016863752.1
XM_017008264.1 1087 Silent Mutation CTG,TTG L15L XP_016863753.1
XM_017008265.1 1087 Silent Mutation CTG,TTG L15L XP_016863754.1
XM_017008266.1 1087 Silent Mutation CTG,TTG L15L XP_016863755.1
XM_017008267.1 1087 Silent Mutation CTG,TTG L15L XP_016863756.1
XM_017008268.1 1087 Silent Mutation CTG,TTG L15L XP_016863757.1
XM_017008269.1 1087 Silent Mutation CTG,TTG L15L XP_016863758.1
XM_017008270.1 1087 Silent Mutation CTG,TTG L15L XP_016863759.1
XM_017008271.1 1087 Silent Mutation CTG,TTG L15L XP_016863760.1
XM_017008272.1 1087 Silent Mutation CTG,TTG L15L XP_016863761.1

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