Product Details

SNP ID: rs200639211
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:183446171 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGAGCAAGATCACGCAAAAACCTCT[A/G]CCAAGACAGAACGTGCATCAGCTCA
Phenotype: MIM: 615914
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CDKN2AIP PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317343.1	663	UTR 3			NP_001304272.1
NM_017632.3	663	Missense Mutation	ACC,GCC	T163A	NP_060102.1