Product Details

SNP ID: rs2286501
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:22817166 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TCGTTCCTCCAGAGCAAACCTGCCT[C/G]TTTGAGATTATACCTATATATATAA
Phenotype: MIM: 607980
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: TOMM7 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019059.3		Intron			NP_061932.1