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SNP ID: rs9941017
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:67227859 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGCCCAAGGGCAAAGTGGGCACGAG[A/G]GGGAAGAAGCAGATATTTGAAGAGA
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

There are no transcripts associated with this gene.

Gene: LOC105369155
Gene Name: uncharacterized LOC105369155

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
XM_011523526.2	253	Intron			XP_011521828.1

Gene: LRRC29
Gene Name: leucine rich repeat containing 29

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001004055.1	253	Intron			NP_001004055.1
NM_012163.2	253	Intron			NP_036295.1
XM_017023126.1	253	Intron			XP_016878615.1
XM_017023127.1	253	Intron			XP_016878616.1
XM_017023128.1	253	Intron			XP_016878617.1
XM_017023129.1	253	Intron			XP_016878618.1
XM_017023130.1	253	Intron			XP_016878619.1
XM_017023131.1	253	Intron			XP_016878620.1
XM_017023132.1	253	Intron			XP_016878621.1
XM_017023133.1	253	Intron			XP_016878622.1
XM_017023134.1	253	Intron			XP_016878623.1

Gene: TMEM208
Gene Name: transmembrane protein 208

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001318217.1	253	UTR 5			NP_001305146.1
NM_014187.3	253	Silent Mutation	AGA,AGG	R10R	NP_054906.2

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