Product Details

SNP ID
rs200544374
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:42096191 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGGGATGGTGGCTCCAAGCATTTG[G/T]GGGGCTGCGGGTGCGAGAGGTGCGG
Phenotype
MIM: 164176
Polymorphism
G/T, Transversion 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_001207025.2 949 Missense Mutation CAC,CCC H185P NP_001193954.1
NM_001207026.1 949 Missense Mutation CAC,CCC H185P NP_001193955.1
NM_001247994.1 949 Missense Mutation CAC,CCC H169P NP_001234923.1
NM_002698.4 949 Missense Mutation CAC,CCC H169P NP_002689.1
XM_005259010.3 949 Missense Mutation CAC,CCC H169P XP_005259067.1
XM_011527040.2 949 Missense Mutation CAC,CCC H207P XP_011525342.1
XM_011527041.2 949 Missense Mutation CAC,CCC H207P XP_011525343.1
XM_011527042.2 949 Missense Mutation CAC,CCC H191P XP_011525344.1
XM_011527043.2 949 Missense Mutation CAC,CCC H306P XP_011525345.2
XM_017026884.1 949 Missense Mutation CAC,CCC H306P XP_016882373.1
XM_017026885.1 949 Missense Mutation CAC,CCC H306P XP_016882374.1
XM_017026886.1 949 Missense Mutation CAC,CCC H294P XP_016882375.1
XM_017026887.1 949 Missense Mutation CAC,CCC H294P XP_016882376.1
XM_017026888.1 949 Missense Mutation CAC,CCC H294P XP_016882377.1
XM_017026889.1 949 Missense Mutation CAC,CCC H294P XP_016882378.1
XM_017026890.1 949 Missense Mutation CAC,CCC H294P XP_016882379.1
XM_017026891.1 949 Missense Mutation CAC,CCC H290P XP_016882380.1
XM_017026892.1 949 Missense Mutation CAC,CCC H284P XP_016882381.1
XM_017026893.1 949 Missense Mutation CAC,CCC H191P XP_016882382.1
XM_017026894.1 949 Missense Mutation CAC,CCC H185P XP_016882383.1
XM_017026895.1 949 Missense Mutation CAC,CCC H185P XP_016882384.1
XM_017026896.1 949 Missense Mutation CAC,CCC H306P XP_016882385.1

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