Product Details

SNP ID: rs145700427
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:49962787 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: GCTGGGCGTGCTTCTCTACGATATG[G/T]TGTGTGGGGACATCCCCTTCGAGCA
Phenotype: MIM: 610580
Polymorphism: G/T, Transversion 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	1168	Missense Mutation	GTG,TTG	V239L	NP_001001852.2