Product Details

SNP ID
rs190207170
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:67230465 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGCATGATGCGCACTTCACGGGCC[A/G]CCTGCGGGGTGTAGCCCAGGTAGAG
Phenotype
MIM: 606881
Polymorphism
A/G, 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 3306 Missense Mutation GCG,GTG A993V NP_001305131.1
NM_013241.2 3306 Missense Mutation GCG,GTG A967V NP_037373.2
XM_006721180.1 3306 Missense Mutation GCG,GTG A498V XP_006721243.1
XM_011523043.2 3306 Missense Mutation GCG,GTG A983V XP_011521345.1
XM_011523044.1 3306 Missense Mutation GCG,GTG A939V XP_011521346.1
XM_011523045.2 3306 Missense Mutation GCG,GTG A900V 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
There are no transcripts associated with this gene.

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