Product Details

SNP ID

rs1605029

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.7:55814224 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTGAATACTTAGAAAACCTTCTCAA[A/G]TAGAATAGGCACAATTGAGCCCAGA

Phenotype

MIM: 612140

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SEPT14 PubMed Links

Additional Information

For this assay, SNP(s) [rs114410924,rs1605030] 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

SEPT14

Gene Name

septin 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_207366.2		Intron			NP_997249.2
XM_011515373.2		Intron			XP_011513675.1

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