Product Details

SNP ID

rs8142355

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.22:31685695 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTTTGCCTCGAGCTCTCCTCTTTCG[C/T]GGGACTGTAAAATCCTGAAATTCTA

Phenotype

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

PRR14L PubMed Links

Additional Information

For this assay, SNP(s) [rs78356740] 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

PRR14L

Gene Name

proline rich 14 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_173566.2	7041	Silent Mutation			NP_775837.2
XM_006724219.3	7041	Silent Mutation			XP_006724282.1
XM_006724220.3	7041	Silent Mutation			XP_006724283.1
XM_006724221.2	7041	Silent Mutation			XP_006724284.1
XM_011530080.2	7041	Silent Mutation			XP_011528382.1
XM_011530081.2	7041	Silent Mutation			XP_011528383.1
XM_017028736.1	7041	Silent Mutation			XP_016884225.1
XM_017028737.1	7041	Silent Mutation			XP_016884226.1

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