Product Details

SNP ID

rs10814585

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.9:37605586 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CCCTGCTAATGGTGAGAAAGGCCAC[C/G]TATCTGATAGGACTTTGGAAATTGC

Phenotype

MIM: 616919

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

FRMPD1 PubMed Links

Additional Information

For this assay, SNP(s) [rs144462695] 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

FRMPD1

Gene Name

FERM and PDZ domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014907.2		Intron			NP_055722.2
XM_011517803.2		Intron			XP_011516105.1
XM_011517804.2		Intron			XP_011516106.1
XM_011517805.2		Intron			XP_011516107.1
XM_011517806.2		Intron			XP_011516108.1
XM_017014480.1		Intron			XP_016869969.1
XM_017014481.1		Intron			XP_016869970.1
XM_017014482.1		Intron			XP_016869971.1

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