Product Details

SNP ID

rs17003770

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:96692571 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCTGTCTTTAATTCTGTAGAAGTA[C/T]CTGGAAAGGTTGACTATACAAGGGT

Phenotype

MIM: 300108

Polymorphism

C/T, Transition 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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