Product Details

SNP ID: rs201755087
Assay Type: Functionally tested
NCBI dbSNP Submissions: 5
Location: Chr.1:180916241 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTGGTCCTGAGCCACAGCTGGATAA[C/T]GGACACCCCCCAAGACCCTGGCCTT
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: KIAA1614 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020950.1	205	Silent Mutation	AAC,AAT	N46N	NP_066001.1