Product Details

SNP ID

rs139222024

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:30721518 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGCTCAGCCTGGCGGCCGCCAAGCA[A/G]CTCCTCCGGTACCGGCTGGCCGAGG

Phenotype

MIM: 602988

Polymorphism

A/G, 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	1140	Silent Mutation	CAA,CAG	Q32Q	NP_001166994.1
NM_002589.2	1140	Silent Mutation	CAA,CAG	Q32Q	NP_002580.2
NM_032456.2	1140	Silent Mutation	CAA,CAG	Q32Q	NP_115832.1
NM_032457.3	1140	Silent Mutation	CAA,CAG	Q32Q	NP_115833.2
XM_005248163.3	1140	Silent Mutation	CAA,CAG	Q32Q	XP_005248220.1
XM_005248164.3	1140	Silent Mutation	CAA,CAG	Q32Q	XP_005248221.1
XM_005248166.3	1140	Silent Mutation	CAA,CAG	Q32Q	XP_005248223.1
XM_011513842.2	1140	Silent Mutation	CAA,CAG	Q32Q	XP_011512144.1
XM_011513843.2	1140	Silent Mutation	CAA,CAG	Q32Q	XP_011512145.1
XM_011513844.2	1140	Silent Mutation	CAA,CAG	Q32Q	XP_011512146.1
XM_017008259.1	1140	Silent Mutation	CAA,CAG	Q32Q	XP_016863748.1
XM_017008260.1	1140	Silent Mutation	CAA,CAG	Q32Q	XP_016863749.1
XM_017008261.1	1140	Silent Mutation	CAA,CAG	Q32Q	XP_016863750.1
XM_017008262.1	1140	Missense Mutation	CAA,CAG	Q32Q	XP_016863751.1
XM_017008263.1	1140	Silent Mutation	CAA,CAG	Q32Q	XP_016863752.1
XM_017008264.1	1140	Silent Mutation	CAA,CAG	Q32Q	XP_016863753.1
XM_017008265.1	1140	Silent Mutation	CAA,CAG	Q32Q	XP_016863754.1
XM_017008266.1	1140	Silent Mutation	CAA,CAG	Q32Q	XP_016863755.1
XM_017008267.1	1140	Silent Mutation	CAA,CAG	Q32Q	XP_016863756.1
XM_017008268.1	1140	Silent Mutation	CAA,CAG	Q32Q	XP_016863757.1
XM_017008269.1	1140	Silent Mutation	CAA,CAG	Q32Q	XP_016863758.1
XM_017008270.1	1140	Silent Mutation	CAA,CAG	Q32Q	XP_016863759.1
XM_017008271.1	1140	Silent Mutation	CAA,CAG	Q32Q	XP_016863760.1
XM_017008272.1	1140	Silent Mutation	CAA,CAG	Q32Q	XP_016863761.1

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