Product Details

SNP ID: rs201567136
Assay Type: Functionally tested
NCBI dbSNP Submissions: 3
Location: Chr.1:93872130 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TTTCTTGTAAAATCTTTTCGGGTCC[A/G]TGCTGGCTCTCATCTTCAGTGCTTT
Phenotype: MIM: 611199
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: DNTTIP2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_014597.4	2067	Missense Mutation	ACG,ATG	T670M	NP_055412.2