Product Details

SNP ID: rs6944634
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:75432493 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: ACTCTATTTCCATCTATATAAAATT[C/G]AAAAACAGGGTACACTATAAAAGGT
Phenotype: MIM: 615754
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: POM121C PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001099415.2		Intron			NP_001092885.2