Product Details

SNP ID

rs4862637

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:186108646 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGAGCCAGAGGCAGAGGATACTGA[G/T]CTCTCTGTCTTCACCTCACTTTCCT

Phenotype

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

FAM149A PubMed Links

Additional Information

For this assay, SNP(s) [rs116191943] 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

FAM149A

Gene Name

family with sequence similarity 149 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001006655.2		Intron			NP_001006656.1
NM_015398.2		Intron			NP_056213.1
XM_005262911.1		Intron			XP_005262968.1
XM_005262912.1		Intron			XP_005262969.1
XM_005262913.1		Intron			XP_005262970.1
XM_011531834.1		Intron			XP_011530136.1
XM_011531835.2		Intron			XP_011530137.1
XM_011531836.1		Intron			XP_011530138.1
XM_017007996.1		Intron			XP_016863485.1
XM_017007997.1		Intron			XP_016863486.1
XM_017007998.1		Intron			XP_016863487.1
XM_017007999.1		Intron			XP_016863488.1
XM_017008000.1		Intron			XP_016863489.1
XM_017008001.1		Intron			XP_016863490.1
XM_017008002.1		Intron			XP_016863491.1
XM_017008003.1		Intron			XP_016863492.1
XM_017008004.1		Intron			XP_016863493.1
XM_017008005.1		Intron			XP_016863494.1
XM_017008006.1		Intron			XP_016863495.1
XM_017008007.1		Intron			XP_016863496.1
XM_017008008.1		Intron			XP_016863497.1

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