Product Details

SNP ID: hCV44668442
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:155033489 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GTGGCGTAAGCTGTTCGGGCAGGAA[C/T]CTGGACCTTCAGCAGAAAAGTATAG
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: FUNDC2 PubMed Links

Gene Details

There are no transcripts associated with this gene.