Product Details

SNP ID: rs11769629
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:22815304 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CACATTCTTGCCCCACTTCTGTATC[A/C]TAAATCACCCAGGGCACAAAAAAGT
Phenotype: MIM: 607980
Polymorphism: A/C, 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