Product Details

SNP ID: rs146505168
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:25616137 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACCATCACACAGTCCCCAGGTTGTA[C/T]TCCGAGAAGATTGCAGCAGTAATAA
Phenotype: MIM: 610763
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: NANP PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152667.2	599	Missense Mutation	ATA,GTA	I179V	NP_689880.1

There are no transcripts associated with this gene.