Product Details

SNP ID

rs148262252

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:49406819 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGAGCCACCTGTTTGGCTTCCAC[C/T]GCTTCTGTGAACTCCTTCCCGAAGG

Phenotype

MIM: 176705

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PHB PubMed Links

Additional Information

For this assay, SNP(s) [rs2233667] 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

PHB

Gene Name

prohibitin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001281496.1	616	Intron			NP_001268425.1
NM_001281497.1	616	Intron			NP_001268426.1
NM_001281715.1	616	Intron			NP_001268644.1
NM_002634.3	616	Intron			NP_002625.1
XM_017024762.1	616	Silent Mutation	GCA,GCG	A182A	XP_016880251.1
XM_017024763.1	616	Intron			XP_016880252.1

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