Product Details

SNP ID: rs2212618
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.18:31508185 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CCAACACCATAAAATGGTATTTTTT[A/G]AGTGACAAATGCTTAGGACCAGTAA
Phenotype: MIM: 125671
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: DSG2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001943.4		Intron			NP_001934.2