Product Details

SNP ID

rs61736483

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:51612393 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGGAGGAGATGCTTGATCTCCGGG[A/G]CTGTCTGGCCAGGGCTTCTTCCTGG

Phenotype

MIM: 604200

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SIGLEC5 PubMed Links

Additional Information

For this assay, SNP(s) [rs3829655] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

SIGLEC5

Gene Name

sialic acid binding Ig like lectin 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003830.3	1633	Silent Mutation	AGC,AGT	S498S	NP_003821.1
XM_011527438.2	1633	Missense Mutation	GCC,GTC	A471V	XP_011525740.1
XM_017027419.1	1633	Silent Mutation	AGC,AGT	S507S	XP_016882908.1

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