Product Details

SNP ID: rs201455550
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.8:24953635 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ATCTGCTCCTCTTGGACATGGCTGG[G/T]GTAGTAGGACGGGAAGGAGCGGGTG
Phenotype: MIM: 162280
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: MIR6841 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_006158.4	1684	Missense Mutation	ACC,CCC	T444P	NP_006149.2