Product Details

SNP ID: rs4799137
Assay Type: Validated
NCBI dbSNP Submissions: NA
Location: Chr.18:80157815 on Build GRCh38
Set Membership: Validated
Context Sequence [VIC/FAM]: ACTCCTCAGCAAAAGCTATTTCTTA[A/C]AAATAGAACTTGCTTTTCACTTAAT
Phenotype: MIM: 608976
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: PARD6G PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_032510.3	3253	UTR 3			NP_115899.1

There are no transcripts associated with this gene.