Product Details

SNP ID

rs201849141

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:111363045 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATGCCACCCCCGCCACGTACAGCC[A/G]CCAGCTGCTGCTCCAGCTCGCGCAC

Phenotype

MIM: 614239

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FAM109A PubMed Links

Additional Information

For this assay, SNP(s) [rs186953579] 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

FAM109A

Gene Name

family with sequence similarity 109 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001177996.1	774	Missense Mutation	GCG,GTG	A141V	NP_001171467.1
NM_001177997.1	774	Missense Mutation	GCG,GTG	A128V	NP_001171468.1
NM_144671.4	774	Missense Mutation	GCG,GTG	A128V	NP_653272.2
XM_006719257.3	774	Missense Mutation	GCG,GTG	A128V	XP_006719320.1
XM_011537976.2	774	Missense Mutation	GCG,GTG	A128V	XP_011536278.1
XM_017018883.1	774	Missense Mutation	GCG,GTG	A128V	XP_016874372.1

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