Product Details

SNP ID: rs2286772
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:17614663 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTTGCGCCATTCCAAACATGGCGGC[C/T]CCACTAGGGGGTATGTTTTCTGGGC
Phenotype: MIM: 170250 MIM: 610311
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: LAP3 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_025205.4	36	Silent Mutation	GCC,GCT	A3A	NP_079481.2