Product Details

SNP ID: rs199831048
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.9:87148838 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCGGACAGAGGAAAGGGGCCTCGCT[C/T]GCAAGGCCCGGGCGGGGAGGCCTGG
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: C9orf170 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001709.2	195	Silent Mutation	CTC,CTT	L36L	NP_001001709.1