Product Details

SNP ID: rs7210156
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:38841208 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: CTGATCAGTTTTCCGCAAAAGGGGC[A/G]GAACCACGTGACTCTGGAAGTAGCT
Phenotype: MIM: 603662
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: C17orf98 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001080465.2	182	Missense Mutation	CCG,CTG	P61L	NP_001073934.1

There are no transcripts associated with this gene.