Product Details

SNP ID

rs148764677

Assay Type

Functionally Tested

NCBI dbSNP Submissions

2

Location

Chr.1:155900532 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCGTACAAGGGCATGGAAAACATC[A/G]TCAATATAGTAGCGGTATGCAGCAG

Phenotype

MIM: 609591

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

RIT1 PubMed Links

Additional Information

For this assay, SNP(s) [rs1749409] 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

RIT1

Gene Name

Ras like without CAAX 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256820.1	719	Silent Mutation	GAC,GAT	D136D	NP_001243749.1
NM_001256821.1	719	Silent Mutation	GAC,GAT	D189D	NP_001243750.1
NM_006912.5	719	Silent Mutation	GAC,GAT	D172D	NP_008843.1

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