Product Details

SNP ID: rs141960676
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.17:79795104 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGGAAACTTTCCTGCCCCGGAAGGG[C/G]TGTCGTCCAGCTTCCTGCCCTTGAG
Phenotype: MIM: 602770
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: CBX2 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_020649.2	819	Missense Mutation	ACC,AGC	T234S	NP_065700.1