Product Details

SNP ID
rs5951168
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:52989241 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
ACAGTGACAAAGCAGGTGGCCACCC[C/G]AGAACACTATAGAGAAAATCTCACC
Phenotype
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
FAM156A PubMed Links

Gene Details

Gene
FAM156A
Gene Name
family with sequence similarity 156 member A
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001242489.1 Intron NP_001229418.1
NM_001242490.1 Intron NP_001229419.1
NM_001242491.1 Intron NP_001229420.1
NM_001242492.1 Intron NP_001229421.1
NM_001242493.1 Intron NP_001229422.1
NM_001242494.1 Intron NP_001229423.1
NM_001242495.1 Intron NP_001229424.1
NM_001242496.1 Intron NP_001229425.1
NM_001242497.1 Intron NP_001229426.1
NM_014138.4 Intron NP_054857.2
XM_006724586.3 Intron XP_006724649.1
XM_006724587.3 Intron XP_006724650.1
XM_011530781.1 Intron XP_011529083.1
XM_011530782.1 Intron XP_011529084.1
XM_011530783.1 Intron XP_011529085.1
XM_011530784.2 Intron XP_011529086.1
XM_017029457.1 Intron XP_016884946.1
XM_017029458.1 Intron XP_016884947.1

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