Product Details

SNP ID

rs7126210

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:47438755 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACCTGAGGTGGAAGATGTGGGAGCA[A/G]GGTAGGGCCTGCAGCCGGCTGTTCT

Phenotype

MIM: 601592

Polymorphism

A/G, Transition 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	1357	Silent Mutation	CCC,CCT	P381P	NP_005046.2
NM_032645.4	1357	Silent Mutation	CCC,CCT	P322P	NP_116034.2
XM_005253042.3	1357	Silent Mutation	CCC,CCT	P363P	XP_005253099.1
XM_005253043.3	1357	Silent Mutation	CCC,CCT	P340P	XP_005253100.1
XM_011520252.1	1357	Silent Mutation	CTG,TTG	L410L	XP_011518554.1

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