Product Details

SNP ID: rs146339729
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:20242118 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGTACTGAGGCCTTGTCAGCGGCAT[C/T]TGGCTGGCAGCACTTGGGAAGCCCC
Phenotype: MIM: 605566
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: MIR1286 PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_023004.5	1216	Missense Mutation	AAT,GAT	N339D	NP_075380.1