Product Details

SNP ID: rs201604881
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:1936823 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGTGGCCCTTGCTCCTGGTGGGGCC[A/G]TGGGGTGAGTGGTGTTCCTTGCGGG
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	1479	Silent Mutation	CAC,CAT	H333H	NP_848663.1