Product Details

SNP ID

rs11767546

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:23686193 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TAGTTTTATAATTTATTCTTACACA[A/G]ATTTAGTGCCACTTTCTAATCTCTG

Phenotype

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FAM221A PubMed Links

Additional Information

For this assay, SNP(s) [rs146135659] 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

FAM221A

Gene Name

family with sequence similarity 221 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001127364.2		Intron			NP_001120836.1
NM_001127365.2		Intron			NP_001120837.1
NM_001300932.1		Intron			NP_001287861.1
NM_199136.4		Intron			NP_954587.2
XM_011515369.2		Intron			XP_011513671.1
XM_011515370.2		Intron			XP_011513672.1
XM_011515371.2		Intron			XP_011513673.1
XM_011515372.2		Intron			XP_011513674.1
XM_017012134.1		Intron			XP_016867623.1
XM_017012135.1		Intron			XP_016867624.1

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