Product Details

SNP ID: rs141235412
Assay Type: Functionally tested
NCBI dbSNP Submissions: 4
Location: Chr.1:93869919 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCATTTGCTGCTTTTTCAGCCATGA[G/T]CTCTGAGTACTTCCTTCGGTTGTAT
Phenotype: MIM: 611199
Polymorphism: G/T, Transversion 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	2261	Missense Mutation	ATC,CTC	I735L	NP_055412.2