Product Details

SNP ID: rs78623586
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:68366222 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGATTGTTTCAGAAATGAGCTGAA[C/T]GTAGTGCCTTCCTTCAGGTGCTTAG
Phenotype: MIM: 173570
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: LOC101927723 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_002664.2		Intron			NP_002655.2