Product Details

SNP ID
rs200445754
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:42093876 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCTTGGGACAACGGTAAGGTCCCC[A/G]CGCCCCCTTGGGGTGTGACCTGAGG
Phenotype
MIM: 164176
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
POU2F2 PubMed Links

Gene Details

Gene
POU2F2
Gene Name
POU class 2 homeobox 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001207025.2 1546 Missense Mutation NP_001193954.1
NM_001207026.1 1546 Missense Mutation NP_001193955.1
NM_001247994.1 1546 Missense Mutation NP_001234923.1
NM_002698.4 1546 Missense Mutation NP_002689.1
XM_005259010.3 1546 Missense Mutation XP_005259067.1
XM_011527040.2 1546 Missense Mutation XP_011525342.1
XM_011527041.2 1546 Missense Mutation XP_011525343.1
XM_011527042.2 1546 Missense Mutation XP_011525344.1
XM_011527043.2 1546 Missense Mutation XP_011525345.2
XM_017026884.1 1546 Missense Mutation XP_016882373.1
XM_017026885.1 1546 Missense Mutation XP_016882374.1
XM_017026886.1 1546 Missense Mutation XP_016882375.1
XM_017026887.1 1546 Missense Mutation XP_016882376.1
XM_017026888.1 1546 Missense Mutation XP_016882377.1
XM_017026889.1 1546 Missense Mutation XP_016882378.1
XM_017026890.1 1546 Missense Mutation XP_016882379.1
XM_017026891.1 1546 Missense Mutation XP_016882380.1
XM_017026892.1 1546 Missense Mutation XP_016882381.1
XM_017026893.1 1546 Missense Mutation XP_016882382.1
XM_017026894.1 1546 Missense Mutation XP_016882383.1
XM_017026895.1 1546 Missense Mutation XP_016882384.1
XM_017026896.1 1546 Missense Mutation XP_016882385.1

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