Product Details

SNP ID
rs12922483
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.16:67248331 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGGGAGGGCCAGGTGCCCCTTGGTT[C/T]GGGAGATGAAGAACAGCCTCCCTCT
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
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001318202.1 783 Intron NP_001305131.1
NM_013241.2 783 Intron NP_037373.2
XM_006721180.1 783 Intron XP_006721243.1
XM_011523043.2 783 Intron XP_011521345.1
XM_011523044.1 783 Intron XP_011521346.1
XM_011523045.2 783 Intron XP_011521347.1
Gene
SLC9A5
Gene Name
solute carrier family 9 member A5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001323971.1 783 Intron NP_001310900.1
NM_001323972.1 783 Intron NP_001310901.1
NM_001323973.1 783 Intron NP_001310902.1
NM_001323974.1 783 Intron NP_001310903.1
NM_001323975.1 783 Intron NP_001310904.1
NM_004594.2 783 Intron NP_004585.1
XM_017023594.1 783 UTR 5 XP_016879083.1

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