Product Details

SNP ID
rs144753004
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:67230434 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAAGCGCAAATTCCCGCAGCGTGTG[C/G]CAGAACTGCATGATGCGCACTTCAC
Phenotype
MIM: 606881
Polymorphism
C/G, Transversion 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 3337 Missense Mutation TGC,TGG C1003W NP_001305131.1
NM_013241.2 3337 Missense Mutation TGC,TGG C977W NP_037373.2
XM_006721180.1 3337 Missense Mutation TGC,TGG C508W XP_006721243.1
XM_011523043.2 3337 Missense Mutation TGC,TGG C993W XP_011521345.1
XM_011523044.1 3337 Missense Mutation TGC,TGG C949W XP_011521346.1
XM_011523045.2 3337 Missense Mutation TGC,TGG C910W 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.

View Full Product Details