Product Details

SNP ID: rs678862
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.6:11544598 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCTAGCCAGTTTTAGAACTCCTACC[A/C]AGTTCAGCCTGCTATTTATTTCCCC
Phenotype
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: TMEM170B PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001100829.2		Intron			NP_001094299.1