Product Details

SNP ID: rs140686158
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.15:64376867 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCTTTTTGCCACTTGGGAGTTGGGC[A/G]CACGCAAACGGGGTTCCCTCCTGCA
Phenotype: MIM: 610696
Polymorphism: A/G, Transition 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	305	Intron			NP_001025160.1
NM_014736.5	305	Missense Mutation	CGC,TGC	R56C	NP_055551.1