Product Details

SNP ID: rs4795939
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:34583039 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GACGCAGTTCCAGCTGGGCCTTAGC[A/G]TCCTGGCTGCCTTCCCTTGGTCTTG
Phenotype: MIM: 616178
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: C17orf102 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_001304438.1		Intron			NP_001291367.1