Product Details

SNP ID

rs2295399

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:92928556 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATAGTTATGTCATCATCAGTGACC[C/T]TGGACTAGTGTTTTGTTTTGTTTTT

Phenotype

MIM: 118910 MIM: 601838

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

CHGA PubMed Links

Additional Information

For this assay, SNP(s) [rs150011146] 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

CHGA

Gene Name

chromogranin A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001275.3		Intron			NP_001266.1
NM_001301690.1		Intron			NP_001288619.1
XM_011536370.1		Intron			XP_011534672.1

Gene

ITPK1

Gene Name

inositol-tetrakisphosphate 1-kinase

There are no transcripts associated with this gene.

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