Product Details

SNP ID

rs77410879

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:47438005 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAAGCCAGGCTTCATGGATGAGCG[C/G]CGGCAGTTGGGACAGCTCCGGGTCC

Phenotype

MIM: 601592

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

RAPSN PubMed Links

Gene Details

Gene

RAPSN

Gene Name

receptor associated protein of the synapse

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005055.4	1423	Silent Mutation	CGC,CGG	R403R	NP_005046.2
NM_032645.4	1423	Silent Mutation	CGC,CGG	R344R	NP_116034.2
XM_005253042.3	1423	Silent Mutation	CGC,CGG	R385R	XP_005253099.1
XM_005253043.3	1423	Silent Mutation	CGC,CGG	R362R	XP_005253100.1
XM_011520252.1	1423	Missense Mutation	CCG,GCG	P432A	XP_011518554.1

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