Product Details

SNP ID
rs145290002
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.X:153670810 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGACAGAGCCTAAGATGTCCCTGTC[A/G]AAGGCTGTGTCCCCAGAGATCCTGG
Phenotype
MIM: 300680
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
PNCK PubMed Links

Gene Details

Gene
PNCK
Gene Name
pregnancy up-regulated nonubiquitous CaM kinase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039582.3 876 Silent Mutation TTC,TTT F359F NP_001034671.3
NM_001135740.1 876 Silent Mutation TTC,TTT F293F NP_001129212.1
XM_005274651.2 876 Silent Mutation TTC,TTT F276F XP_005274708.1
XM_006724809.3 876 Silent Mutation TTC,TTT F276F XP_006724872.1
XM_011531107.2 876 Silent Mutation TTC,TTT F276F XP_011529409.2
XM_011531108.2 876 Silent Mutation TTC,TTT F294F XP_011529410.1
XM_011531110.2 876 Silent Mutation TTC,TTT F276F XP_011529412.1
XM_011531111.2 876 Silent Mutation TTC,TTT F276F XP_011529413.1
XM_011531112.2 876 Silent Mutation TTC,TTT F276F XP_011529414.1
XM_017029277.1 876 Silent Mutation TTC,TTT F359F XP_016884766.1
XM_017029278.1 876 Silent Mutation TTC,TTT F276F XP_016884767.1
XM_017029279.1 876 Silent Mutation TTC,TTT F276F XP_016884768.1
XM_017029280.1 876 Intron XP_016884769.1

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