Product Details

SNP ID

rs4825177

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:143715801 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

ACCCCTTTGTCTAGGATCTCCAAGT[C/T]GTTAACCAGGCCGTGGTACCAATCC

Phenotype

MIM: 300665

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SPANXN2 PubMed Links

Gene Details

Gene

SPANXN2

Gene Name

SPANX family member N2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001009615.2		Intron			NP_001009615.1

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