Product Details

SNP ID: rs16864974
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:223597489 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CCCTTCCCTTTTCTGCCTTTTCTTG[A/G]TTGAGGTATTCCAGCACTTTCATTA
Phenotype: MIM: 118930
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: SCG2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_003469.4	2023	Silent Mutation	AAC,AAT	N598N	NP_003460.2