Product Details

SNP ID

rs6773473

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:68736541 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTGACTTACTGGAGACCATCTTAC[C/T]TTTAGCTTTTCTGTGTTTTGATGCT

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FAM19A4 PubMed Links

Additional Information

For this assay, SNP(s) [rs77929180] 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

FAM19A4

Gene Name

family with sequence similarity 19 member A4, C-C motif chemokine like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001005527.2		Intron			NP_001005527.1
NM_182522.4		Intron			NP_872328.1
XM_011533371.1		Intron			XP_011531673.1
XM_011533372.1		Intron			XP_011531674.1

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