Product Details

SNP ID: rs2009192
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.3:139940740 on Build GRCh38
Set Membership: Validated
Context Sequence [VIC/FAM]: GGCTTGACTTGTTTGTAAAAAGACA[C/T]GCTTTTTTTCACTAGTCTATGGATG
Phenotype: MIM: 611323
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CLSTN2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_022131.2		Intron			NP_071414.2
XM_017007022.1		Intron			XP_016862511.1