Product Details

SNP ID
rs6631282
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:14885199 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTCAGAGCTTTTGCAAACATTCAC[C/G]ACATACTAAGTCATAAAGGGGGTCT
Phenotype
Polymorphism
C/G, Transversion Substitution
Allele Nomenclature
Literature Links
MOSPD2 PubMed Links

Gene Details

Gene
MOSPD2
Gene Name
motile sperm domain containing 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001177475.1 Intron NP_001170946.1
NM_152581.3 Intron NP_689794.1
XM_005274451.1 Intron XP_005274508.1

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