Product Details

SNP ID
rs12971184
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.18:36300722 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTCTCCTGCACATTCAAGCCCCTGA[A/G]GGAGTCAACTTTTTTTTTTTCTCTT
Phenotype
MIM: 609691
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
FHOD3 PubMed Links

Gene Details

Gene
FHOD3
Gene Name
formin homology 2 domain containing 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001281739.2 Intron NP_001268668.1
NM_001281740.2 Intron NP_001268669.1
NM_025135.4 Intron NP_079411.2
XM_005258349.1 Intron XP_005258406.1
XM_005258354.1 Intron XP_005258411.1
XM_005258355.1 Intron XP_005258412.1
XM_011526189.1 Intron XP_011524491.1
XM_011526190.1 Intron XP_011524492.1
XM_011526192.1 Intron XP_011524494.1
XM_011526193.2 Intron XP_011524495.1
XM_011526195.1 Intron XP_011524497.1
XM_011526196.1 Intron XP_011524498.1
XM_011526197.1 Intron XP_011524499.1
XM_017026006.1 Intron XP_016881495.1
XM_017026007.1 Intron XP_016881496.1
XM_017026008.1 Intron XP_016881497.1
XM_017026009.1 Intron XP_016881498.1
XM_017026010.1 Intron XP_016881499.1

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