Product Details

SNP ID

rs5949979

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.X:96698519 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

GTGTTGACTTGTGACGAGTAATAGA[G/C]CCCTAAACTACGGGCGTTAAGTGCC

Phenotype

MIM: 300108

Polymorphism

G/C, Transversion substitution

Allele Nomenclature

Literature Links

DIAPH2 PubMed Links

Gene Details

Gene

DIAPH2

Gene Name

diaphanous related formin 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006729.4		Intron			NP_006720.1
NM_007309.3		Intron			NP_009293.1

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