Product Details

SNP ID: rs3827478
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:120428577 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TAAGGAAGCCCAAGGCCACACCCAC[C/T]GCAACAGGAATAAGAAAGTTGAGGT
Phenotype: MIM: 309060
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: LAMP2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001122606.1	4159	Silent Mutation	GCA,GCG	A381A	NP_001116078.1
NM_002294.2	4159	UTR 3			NP_002285.1
NM_013995.2	4159	Intron			NP_054701.1

There are no transcripts associated with this gene.