Product Details

SNP ID: rs148191398
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:1936786 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TTCCCCGGCTTCCTGTGGCCGGGCC[A/G]GGGGCCGTGCGGGTGGCCCTTGCTC
Phenotype: MIM: 610461
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: RTN4RL1 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_178568.3	1516	Missense Mutation	CGG,TGG	R346W	NP_848663.1