Product Details

SNP ID

rs4385489

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:118956103 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCTGGTTTGCAGACTGCCAACTTT[A/G]CCTTGCAACCTTACGTGGCAGAAAG

Phenotype

MIM: 607620 MIM: 602643

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

COLEC10 PubMed Links

Additional Information

For this assay, SNP(s) [rs75728195] are located under a primer 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

COLEC10

Gene Name

collectin subfamily member 10

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001324095.1		Intron			NP_001311024.1
NM_006438.4		Intron			NP_006429.2
XM_005250756.3		Intron			XP_005250813.1

Gene

TNFRSF11B

Gene Name

TNF receptor superfamily member 11b

There are no transcripts associated with this gene.

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