Product Details

SNP ID
rs2066192
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:59669448 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGTGATCAGAAGAGAGCTCCTGCAC[A/G]TGCCTCACCCCTTCCCCAACACCTA
Phenotype
MIM: 614567
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
DIAPH3 PubMed Links

Gene Details

Gene
DIAPH3
Gene Name
diaphanous related formin 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001042517.1 Intron NP_001035982.1
NM_001258366.1 Intron NP_001245295.1
NM_001258367.1 Intron NP_001245296.1
NM_001258368.1 Intron NP_001245297.1
NM_001258369.1 Intron NP_001245298.1
NM_001258370.1 Intron NP_001245299.1
NM_030932.3 Intron NP_112194.2
XM_006719876.1 Intron XP_006719939.1
XM_011535258.2 Intron XP_011533560.1
XM_011535263.2 Intron XP_011533565.1
XM_011535265.2 Intron XP_011533567.1
XM_017020789.1 Intron XP_016876278.1

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