Product Details

SNP ID: rs4795938
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:34581045 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GGGCCAAGTCGTCGTCGACTGTTGC[C/T]CTCTCGGACCCCTCCCGCCCCCGCC
Phenotype: MIM: 616178
Polymorphism: C/T, 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	297	UTR 5			NP_001291367.1