Product Details

SNP ID: hCV27839786
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.1:40258150 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CGCGCAGAGGGAGGGATGGGGGCGG[C/G]TATCGGCGTAGGGGCCCTCGGAAAG
Phenotype: MIM: 606480
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: TMCO2 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_005857.4	101	UTR 5			NP_005848.2