Product Details

SNP ID: rs1319915
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.8:97776258 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: TAATTCTCCGGGTGCCGCGTCCGCA[C/T]TTCCCCCGGCTGGGCCAGCGCCGAC
Phenotype: MIM: 613296
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: LAPTM4B PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_018407.4		Intron			NP_060877.3