Product Details

SNP ID

rs150018904

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:67229875 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTCTTGGTCACTGACTGCACCAG[A/G]AGGTCCATGATCTCATCTGATGTAT

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	3736	Silent Mutation	CTC,CTT	L1136L	NP_001305131.1
NM_013241.2	3736	Silent Mutation	CTC,CTT	L1110L	NP_037373.2
XM_006721180.1	3736	Silent Mutation	CTC,CTT	L641L	XP_006721243.1
XM_011523043.2	3736	Silent Mutation	CTC,CTT	L1126L	XP_011521345.1
XM_011523044.1	3736	Silent Mutation	CTC,CTT	L1082L	XP_011521346.1
XM_011523045.2	3736	Silent Mutation	CTC,CTT	L1043L	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	3736	Intron			NP_001305146.1
NM_014187.3	3736	Intron			NP_054906.2

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