Product Details

SNP ID

rs7236292

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.18:322109 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTGCTTTGGGACAGTTAGATGAAT[A/G]ACTTTCTAATGTGTACTGGAATGCT

Phenotype

MIM: 607621

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

COLEC12 PubMed Links

Additional Information

For this assay, SNP(s) [rs146869750] 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

COLEC12

Gene Name

collectin subfamily member 12

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_130386.2		Intron			NP_569057.1
XM_011525741.2		Intron			XP_011524043.1

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