Product Details

SNP ID

rs139805699

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:100430865 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCAGCCGGAGGGAGTGAGAGTCAC[C/T]CCGTGCCGCCCACAGCCCCTCTCAC

Phenotype

MIM: 611478

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

MEPCE PubMed Links

Additional Information

For this assay, SNP(s) [rs6962151] 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

MEPCE

Gene Name

methylphosphate capping enzyme

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001194990.1	502	UTR 5			NP_001181919.1
NM_001194991.1	502	Intron			NP_001181920.1
NM_001194992.1	502	Intron			NP_001181921.1
NM_019606.5	502	Missense Mutation	CCC,TCC	P283S	NP_062552.2
XM_011516410.2	502	Intron			XP_011514712.1

Gene

PPP1R35

Gene Name

protein phosphatase 1 regulatory subunit 35

There are no transcripts associated with this gene.

Gene

ZCWPW1

Gene Name

zinc finger CW-type and PWWP domain containing 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001258008.1	502	Intron			NP_001244937.1
NM_017984.4	502	Intron			NP_060454.3

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