Product Details

SNP ID: rs2281023
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:27309886 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGCTCCTTGGGATAGTGGGAAAGGT[G/T]GCCTTGAGCTTGATCCCAAGGGACT
Phenotype
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: LOC105375107 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_033482.3	2347	Missense Mutation			NP_258443.2