Product Details

SNP ID
rs149993932
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.22:38059234 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCCTAGCTTGCTTTCCTTTCTAG[C/T]GGAATCCCGACTGTGCCTGGGAAGG
Phenotype
MIM: 605926
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
PICK1 PubMed Links

Gene Details

Gene
PICK1
Gene Name
protein interacting with PRKCA 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001039583.1 23 Silent Mutation CTC,CTT L14L NP_001034672.1
NM_001039584.1 23 Silent Mutation CTC,CTT L14L NP_001034673.1
NM_012407.3 23 Silent Mutation CTC,CTT L14L NP_036539.1
XM_006724379.2 23 UTR 5 XP_006724442.1
XM_006724380.2 23 UTR 5 XP_006724443.1
XM_011530517.2 23 Silent Mutation CTC,CTT L14L XP_011528819.1
XM_017029090.1 23 Intron XP_016884579.1
XM_017029091.1 23 Intron XP_016884580.1
XM_017029092.1 23 UTR 5 XP_016884581.1
XM_017029093.1 23 Intron XP_016884582.1
XM_017029094.1 23 Intron XP_016884583.1
XM_017029095.1 23 UTR 5 XP_016884584.1

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