Product Details

SNP ID: rs114764669
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:44249781 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTGCCGGAAGAAGCCAGGTTTTCTC[C/T]GAGCATGTGGGTTTTGTCTTCTGAA
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: KIAA1644 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001099294.1		Intron			NP_001092764.1
XM_005261790.3		Intron			XP_005261847.1