Product Details

SNP ID: rs2296662
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:35776992 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCAGTCCTGGGCTCGCTTCCCTCCC[C/G]AAACTGCTCACAGGCAAACCCACCC
Phenotype
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: CLPSL1 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286550.1		Intron			NP_001273479.1
NM_207409.3		Intron			NP_997292.2