Product Details

SNP ID: rs138160608
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.15:64376809 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGGAATCTGATTCTCTTTTTCAGAA[A/T]CTTTAGGGGACAACCTAAAGAATTC
Phenotype: MIM: 610696
Polymorphism: A/T, Transversion substitution
Allele Nomenclature
Literature Links: KIAA0101 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001029989.2	363	Intron			NP_001025160.1
NM_014736.5	363	Missense Mutation	GAT,GTT	D75V	NP_055551.1