Product Details

SNP ID: rs139268901
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.22:49961771 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGCTCAAGCTCATCGACTTCGGTTC[C/G]GGTGCGCTGCTCAAGGACACGGTCT
Phenotype: MIM: 610580
Polymorphism: C/G, 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	1029	Silent Mutation	TCC,TCG	S192S	NP_001001852.2