Product Details

SNP ID

rs79989624

Assay Type

Functionally tested

NCBI dbSNP Submissions

2

Location

Chr.1:157578495 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTACCTTCCTCTTCTTCTCCCAGCT[G/T]AGTAGTCTGGATCTCAGAGTATACC

Phenotype

MIM: 605876

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

FCRL4 PubMed Links

Gene Details

Gene

FCRL4

Gene Name

Fc receptor like 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031282.2	1520	Missense Mutation	AAG,CAG	K470Q	NP_112572.1
XM_011510034.1	1520	Missense Mutation	AAG,CAG	K469Q	XP_011508336.1

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