Product Details

SNP ID: hCV11326197
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:160711894 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGAAGATACGTGAAATTCAAATGTT[A/G]CAACTTGCCTATTATTTATTTTAGT
Phenotype: MIM: 173350
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: PLG PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000301.3		Intron			NP_000292.1
NM_001168338.1		Intron			NP_001161810.1