Product Details

SNP ID

rs11051378

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:31297906 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTCCTCATAATCTGGAAAAAAGTA[A/G]GCTGTCAGCATTGTTTGATTCATTT

Phenotype

MIM: 615027

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FAM60A PubMed Links

Additional Information

For this assay, SNP(s) [rs200154377] 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

FAM60A

Gene Name

family with sequence similarity 60 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135811.1		Intron			NP_001129283.1
NM_001135812.1		Intron			NP_001129284.1
NM_021238.2		Intron			NP_067061.1
XM_011520803.2		Intron			XP_011519105.1
XM_017019758.1		Intron			XP_016875247.1
XM_017019759.1		Intron			XP_016875248.1
XM_017019760.1		Intron			XP_016875249.1
XM_017019761.1		Intron			XP_016875250.1
XM_017019762.1		Intron			XP_016875251.1

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