Product Details

SNP ID

rs944627

Assay Type

Functionally tested

NCBI dbSNP Submissions

37

Location

Chr.1:157680749 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GATGCTCCAGATCTGGGAATAAATC[A/G]GGTTGCTATCTCCAGGATTTACTGT

Phenotype

MIM: 606510

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FCRL3 PubMed Links

Gene Details

Gene

FCRL3

Gene Name

Fc receptor like 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001320333.1	2286	Missense Mutation	CCG,CTG	P660L	NP_001307262.1
NM_052939.3	2286	Missense Mutation	CCG,CTG	P660L	NP_443171.2
XM_006711145.1	2286	Missense Mutation	CCG,CTG	P660L	XP_006711208.1

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