Product Details

SNP ID

rs1448865

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.X:44149116 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

TGTCATATGACTCTGTAGAACCTCC[C/T]GTGGAGTAAGAAGGGTATATTTTCC

Phenotype

MIM: 300817

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

EFHC2 PubMed Links

Gene Details

Gene

EFHC2

Gene Name

EF-hand domain containing 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025184.3		Intron			NP_079460.2
XM_006724562.2		Intron			XP_006724625.1

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