Product Details

SNP ID

rs115907662

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:214414211 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAGGGGGATGGCTCTTCATATTCA[A/T]GAAGCTTGCATACTTCTGTTGGTCA

Phenotype

MIM: 612173

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

SPAG16 PubMed Links

Gene Details

Gene

SPAG16

Gene Name

sperm associated antigen 16

There are no transcripts associated with this gene.

Gene

VWC2L

Gene Name

von Willebrand factor C domain containing protein 2-like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080500.2	148	Missense Mutation	CAA,CAT	Q6H	NP_001073969.1

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