Product Details

SNP ID: rs1006722
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:17617090 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CATATAGGTGTGGACATCAAAGAAG[A/G]CTTCCCAGAGAGCAGGAAAGCCAAA
Phenotype: MIM: 170250 MIM: 610311
Polymorphism: A/G, 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		Intron			NP_079481.2