Product Details

SNP ID: rs140828478
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.9:19116584 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CACCTTGGATGTTGGACAGGAGGGT[A/G]TGGCACGTGGTCTGGAGCTGCTGAG
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	1000	Intron			NP_001113.2
XM_017014259.1	1000	Silent Mutation	CAC,CAT	H326H	XP_016869748.1