Product Details

SNP ID: rs4978888
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.9:110201422 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GGGACAGTGAGCTTCTTCTCTCCTT[A/G]TTAATCCAAACAGCATTGACCATCG
Phenotype
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: C9orf152 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001012993.2	800	Silent Mutation	AAC,AAT	N82N	NP_001013011.2