Product Details

SNP ID

rs114513875

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:81432632 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAATGTATAAGGCAAAAAAAAGCT[G/T]ATAAAATGTAAGCCATATGATGCTG

Phenotype

MIM: 614532

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

RASGEF1B PubMed Links

Additional Information

For this assay, SNP(s) [rs112445543] 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

RASGEF1B

Gene Name

RasGEF domain family member 1B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001300735.1		Intron			NP_001287664.1
NM_001300736.1		Intron			NP_001287665.1
NM_152545.2		Intron			NP_689758.1
XM_017007812.1		Intron			XP_016863301.1
XM_017007813.1		Intron			XP_016863302.1

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