Product Details

SNP ID: rs145283880
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.15:64395472 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GAAAGGGAGAAACAGACAGGAAGTT[C/T]CTGCATTTACTGAACCTGACACGAC
Phenotype: MIM: 610696 MIM: 604501
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: KIAA0101 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321924.1	406	UTR 5			NP_001308853.1
NM_016213.4	406	Missense Mutation	CCT,TCT	P116S	NP_057297.2