Product Details

SNP ID: rs144722957
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:17614671 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ATTCCAAACATGGCGGCTCCACTAG[A/G]GGGTATGTTTTCTGGGCAGCCACCC
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	44	Missense Mutation	GAG,GGG	E6G	NP_079481.2