Product Details
- SNP ID
-
rs147695707
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:57236030 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TGCCTGCGCACCTGCTCTGGCCACA[A/G]CAGAGCATGGAGGTGCAGGCCTGGC
- Phenotype
-
MIM: 600052
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
APLNR
PubMed Links
Gene Details
- Gene
- APLNR
- Gene Name
- apelin receptor
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_005161.4 |
1424 |
Silent Mutation |
TGC,TGT |
C325C |
NP_005152.1 |
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