Product Details

SNP ID

rs145142983

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:41497580 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTTATGCAGAAGCAGAGAAGCTCGG[C/T]GGCCAGTCATATCTCGAAGGTTGTT

Phenotype

MIM: 609453

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

GOLGA7 PubMed Links

Additional Information

For this assay, SNP(s) [rs17656952] 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

GOLGA7

Gene Name

golgin A7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001002296.1		Intron			NP_001002296.1
NM_001174124.1		Intron			NP_001167595.1
NM_016099.2		Intron			NP_057183.2

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