Product Details

SNP ID
rs199532825
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.16:67229105 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCGACAGGAGCGGCGGCAGATGAAG[C/T]GGTTATAGCCATTGACATTGTGGCC
Phenotype
MIM: 606881
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
FHOD1 PubMed Links

Gene Details

Gene
FHOD1
Gene Name
formin homology 2 domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318202.1 737 Intron NP_001305131.1
NM_013241.2 737 Intron NP_037373.2
XM_006721180.1 737 Intron XP_006721243.1
XM_011523043.2 737 Intron XP_011521345.1
XM_011523044.1 737 Intron XP_011521346.1
XM_011523045.2 737 Intron XP_011521347.1
Gene
LOC105369155
Gene Name
uncharacterized LOC105369155
There are no transcripts associated with this gene.

Gene
LRRC29
Gene Name
leucine rich repeat containing 29
There are no transcripts associated with this gene.

Gene
TMEM208
Gene Name
transmembrane protein 208
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318217.1 737 Missense Mutation CGG,TGG R102W NP_001305146.1
NM_014187.3 737 Missense Mutation CGG,TGG R172W NP_054906.2

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