Product Details

SNP ID

rs139955742

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:67229821 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTTGCGGTTGCCGCGGGAACGCTT[C/G]CGTTCCCTAGCAGCTAAGGCACGAG

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	3790	Silent Mutation	CGC,CGG	R1154R	NP_001305131.1
NM_013241.2	3790	Silent Mutation	CGC,CGG	R1128R	NP_037373.2
XM_006721180.1	3790	Silent Mutation	CGC,CGG	R659R	XP_006721243.1
XM_011523043.2	3790	Silent Mutation	CGC,CGG	R1144R	XP_011521345.1
XM_011523044.1	3790	Silent Mutation	CGC,CGG	R1100R	XP_011521346.1
XM_011523045.2	3790	Silent Mutation	CGC,CGG	R1061R	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	3790	Intron			NP_001305146.1
NM_014187.3	3790	Intron			NP_054906.2

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