Product Details

SNP ID: rs111721329
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:139940394 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CATCTGAGACTCAGTTTCCTCATCT[A/C]TAAAATGGGGATACAGAGATCTACC
Phenotype: MIM: 611323
Polymorphism: A/C, Transversion 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