Product Details

SNP ID
rs3750200
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:70111799 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTTTCACCCTGCCACAAATAAACAA[A/T]CAATCAAATTTCAAGGAAAAACTTC
Phenotype
MIM: 601993
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
NCOA2 PubMed Links

Gene Details

Gene
NCOA2
Gene Name
nuclear receptor coactivator 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321703.1 6692 UTR 3 NP_001308632.1
NM_001321707.1 6692 UTR 3 NP_001308636.1
NM_001321711.1 6692 UTR 3 NP_001308640.1
NM_001321712.1 6692 UTR 3 NP_001308641.1
NM_001321713.1 6692 UTR 3 NP_001308642.1
NM_006540.3 6692 UTR 3 NP_006531.1
XM_017012961.1 6692 UTR 3 XP_016868450.1
XM_017012962.1 6692 UTR 3 XP_016868451.1
XM_017012963.1 6692 UTR 3 XP_016868452.1
XM_017012964.1 6692 UTR 3 XP_016868453.1
XM_017012965.1 6692 UTR 3 XP_016868454.1
XM_017012966.1 6692 UTR 3 XP_016868455.1
XM_017012967.1 6692 UTR 3 XP_016868456.1
XM_017012968.1 6692 UTR 3 XP_016868457.1
XM_017012969.1 6692 UTR 3 XP_016868458.1
XM_017012970.1 6692 UTR 3 XP_016868459.1
XM_017012971.1 6692 UTR 3 XP_016868460.1
XM_017012972.1 6692 UTR 3 XP_016868461.1
XM_017012973.1 6692 Intron XP_016868462.1

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