Product Details

SNP ID

rs200242493

Assay Type

Functionally Tested

NCBI dbSNP Submissions

9

Location

Chr.1:152515434 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGCCAAAGGCTTTTCCAAGGGGTC[G/T]TCCCAGGGCCCCGCTCCGTGTCCCG

Phenotype

MIM: 612619

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

CRCT1 PubMed Links

Additional Information

For this assay, SNP(s) [rs73004856] 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

CRCT1

Gene Name

cysteine rich C-terminal 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019060.2	210	Silent Mutation	TCG,TCT	S17S	NP_061933.1
XM_011509656.2	210	Silent Mutation	TCG,TCT	S17S	XP_011507958.1

Gene

LCE5A

Gene Name

late cornified envelope 5A

There are no transcripts associated with this gene.

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