Product Details

SNP ID: rs141685840
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.9:19116632 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAGTCAGGTTGCGGGCAATTGCAAG[A/G]GTACGTGACTCAATGTGCTAAAAAT
Phenotype: MIM: 103195
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: PLIN2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001122.3	952	Intron			NP_001113.2
XM_017014259.1	952	Silent Mutation	ACC,ACT	T310T	XP_016869748.1