Product Details

SNP ID: rs146022178
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.16:25692989 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGGGGCGGCGCCGTCAGCACCCCCG[A/G]CTATGGGGAGAAGAAGCTGCCACAG
Phenotype: MIM: 604059
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: HS3ST4 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006040.2	964	Missense Mutation	GAC,GGC	D191G	NP_006031.2