Product Details

SNP ID: rs3808172
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.7:118232955 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TTTGGTGGGCTTAAAGCTATTTAGC[C/T]CTGTGTTATGTTTGGATTGAGGGCT
Phenotype: MIM: 610731
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ANKRD7 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019644.3		Intron			NP_062618.2