Product Details

SNP ID: rs9521974
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.13:110882133 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAGCACCCTCCTATCCGAGCCCTTT[C/T]CAGGGGTGGGGACACTTGACCCTCC
Phenotype
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: ANKRD10 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001286721.1		Intron			NP_001273650.1
NM_017664.3		Intron			NP_060134.2