Product Details

SNP ID: rs12963302
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.18:31320671 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCAAACACATTTTGTTAATTCTGCA[C/T]CTATTTTTCATTCTTCTTTTTGTTT
Phenotype: MIM: 125670
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: DSG1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001942.3		Intron			NP_001933.2