Product Details

SNP ID

rs115213262

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.3:172893879 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATGTAGTCTGAATCAAGGAGAGAG[A/G]ATTAGGTGTGTTTATATGGGTTTGC

Phenotype

MIM: 609856

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SPATA16 PubMed Links

Additional Information

For this assay, SNP(s) [rs59163576] 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

SPATA16

Gene Name

spermatogenesis associated 16

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_031955.5		Intron			NP_114161.3
XM_006713778.2		Intron			XP_006713841.1
XM_017007308.1		Intron			XP_016862797.1

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