Product Details

SNP ID
rs144815381
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.16:67229671 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGCCAGGACCCTTGCTTAGTCCCA[G/T]TGCCTGCACCAGGTCATCTCCGAGC
Phenotype
MIM: 606881
Polymorphism
G/T, 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 3866 Missense Mutation ATG,CTG M1180L NP_001305131.1
NM_013241.2 3866 Missense Mutation ATG,CTG M1154L NP_037373.2
XM_006721180.1 3866 Missense Mutation ATG,CTG M685L XP_006721243.1
XM_011523043.2 3866 Missense Mutation ATG,CTG M1170L XP_011521345.1
XM_011523044.1 3866 Missense Mutation ATG,CTG M1126L XP_011521346.1
XM_011523045.2 3866 Missense Mutation ATG,CTG M1087L 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 3866 Intron NP_001305146.1
NM_014187.3 3866 Intron NP_054906.2

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