Product Details

SNP ID

rs933832

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.8:41533235 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATATGAGCTGCCAAAGAAACACTTT[A/C]TGTAAAGTTCAAACTTGCAAAATTA

Phenotype

MIM: 610611

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

GINS4 PubMed Links

Additional Information

For this assay, SNP(s) [rs75925561] 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

GINS4

Gene Name

GINS complex subunit 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032336.2		Intron			NP_115712.1
XM_005273659.3		Intron			XP_005273716.1

Gene

LOC102723729

Gene Name

uncharacterized LOC102723729

There are no transcripts associated with this gene.

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