Product Details

SNP ID: rs184673082
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:1936560 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAGGGAGGCCCCCAGGGAACTGGCC[A/G]AGGAGGCCTGCTGCACCCCGCTGGG
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	1742	Missense Mutation	TCG,TTG	S421L	NP_848663.1