Product Details

SNP ID
rs4533277
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.16:67254113 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TATATGTTAGGCATTGGCTAAGGAA[C/T]TTTTTGAGGTAGATATTGTTATTAG
Phenotype
MIM: 606881 MIM: 600477
Polymorphism
C/T, 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
SLC9A5
Gene Name
solute carrier family 9 member A5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001323971.1 Intron NP_001310900.1
NM_001323972.1 Intron NP_001310901.1
NM_001323973.1 Intron NP_001310902.1
NM_001323974.1 Intron NP_001310903.1
NM_001323975.1 Intron NP_001310904.1
NM_004594.2 Intron NP_004585.1
XM_017023594.1 Intron XP_016879083.1

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