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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