Product Details

SNP ID: rs146220002
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:49961765 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCGGAGAGCTCAAGCTCATCGACTT[C/T]GGTTCGGGTGCGCTGCTCAAGGACA
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	1023	Silent Mutation	TTC,TTT	F190F	NP_001001852.2