Product Details

SNP ID: rs6662000
Assay Type: Validated
NCBI dbSNP Submissions: 35
Location: Chr.1:34172247 on Build GRCh38
Set Membership: Validated
Context Sequence [VIC/FAM]: TTCTACCTCACTGGACCACTACTGC[C/T]ACCACCATATTCTTTTATTCTGTCA
Phenotype: MIM: 608398
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: C1orf94 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001134734.1		Intron			NP_001128206.1
NM_032884.4		Intron			NP_116273.2

There are no transcripts associated with this gene.