Product Details

SNP ID: rs56188169
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:49962753 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACCGCTACCACGGGCGCTCGGCCAC[C/T]GTGTGGTCGCTGGGCGTGCTTCTCT
Phenotype: MIM: 610580
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: MIR6821 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_001001852.3	1134	Silent Mutation	ACC,ACT	T227T	NP_001001852.2