Product Details

SNP ID: rs6563
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.9:136494732 on Build GRCh38
Set Membership: HapMap Validated
Context Sequence [VIC/FAM]: CGGCTAAGGCTCCCCGAGCTGAGCC[A/G]AGTCTGACGTCCCTCACTGGCATGA
Phenotype: MIM: 190198
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: C9orf163 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_017617.4	9007	UTR 3			NP_060087.3
XM_011518717.2	9007	Intron			XP_011517019.2