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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