Product Details

SNP ID

rs12598966

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.16:15867499 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCAATGTTAGTACTTTTCTGTTCCT[C/T]CTTTCTTAGGTGGTCATCTGAAATG

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

FOPNL PubMed Links

Additional Information

For this assay, SNP(s) [rs115194694] 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

FOPNL

Gene Name

FGFR1OP N-terminal like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001304497.1	332	Missense Mutation	AAG,GAG	K82E	NP_001291426.1
NM_001304498.1	332	UTR 3			NP_001291427.1
NM_001304499.1	332	Missense Mutation	AAG,GAG	K180E	NP_001291428.1
NM_001304500.1	332	Missense Mutation	AAG,GAG	K90E	NP_001291429.1
NM_001304502.1	332	UTR 3			NP_001291431.1
NM_144600.3	332	Missense Mutation	AAG,GAG	K156E	NP_653201.1

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