Product Details

SNP ID

rs369173452

Assay Type

Functionally Tested

NCBI dbSNP Submissions

2

Location

Chr.2:85344095 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTCATAGTCACTGCCCCGCTTTCC[C/G]TTCAGCTCCGCCTGCCACTCCTCAA

Phenotype

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

RETSAT PubMed Links

Gene Details

Gene

RETSAT

Gene Name

retinol saturase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017750.3	1628	Missense Mutation	AAC,AAG	N479K	NP_060220.3

View Full Product Details