Product Details

SNP ID

rs147072100

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:9867257 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGGAGGTGCCAAGCAGTACGTGGCC[C/T]GTGGCCTGCATGCTGAAGAGGGCCC

Phenotype

MIM: 612120

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CIDEC PubMed Links

Additional Information

For this assay, SNP(s) [rs17222536] 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

CIDEC

Gene Name

cell death inducing DFFA like effector c

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199551.1	680	Silent Mutation	ACA,ACG	T208T	NP_001186480.1
NM_001199552.1	680	Silent Mutation	ACA,ACG	T198T	NP_001186481.1
NM_001199623.1	680	Silent Mutation	ACA,ACG	T211T	NP_001186552.1
NM_001321142.1	680	Silent Mutation	ACA,ACG	T198T	NP_001308071.1
NM_001321143.1	680	Silent Mutation	ACA,ACG	T124T	NP_001308072.1
NM_001321144.1	680	Silent Mutation	ACA,ACG	T124T	NP_001308073.1
NM_022094.3	680	Silent Mutation	ACA,ACG	T198T	NP_071377.2

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