Product Details

SNP ID
rs199681727
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:143132181 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACCCTGCTCCTGGTTCTCTGCCTGC[A/T]GTTGGGGGCCAACAAAGCTCAGGAC
Phenotype
MIM: 176720
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
PIP PubMed Links

Gene Details

Gene
PIP
Gene Name
prolactin induced protein
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002652.2 101 Missense Mutation CAG,CTG Q22L NP_002643.1

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