Product Details

SNP ID: rs116221847
Assay Type: Functionally tested
NCBI dbSNP Submissions: 12
Location: Chr.1:109214455 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CATGCCGGGGCGGGAGGTTGTGGGG[G/T]CTACGCGGCTTTCCTAACACGAATC
Phenotype: MIM: 611298 MIM: 607529
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: KIAA1324 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_006513.3		Intron			NP_006504.2
XM_006710813.2		Intron			XP_006710876.1