Product Details
- SNP ID
-
rs141189708
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:223597859 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCAGGCAGCTTTGGGAAGCTGGTTC[A/G]ATCTAGATCTTCCAGCACCATAAGG
- Phenotype
-
MIM: 118930
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
SCG2
PubMed Links
Gene Details
- Gene
- SCG2
- Gene Name
- secretogranin II
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_003469.4 |
1653 |
Missense Mutation |
TCG,TTG |
S475L |
NP_003460.2 |
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