Product Details

SNP ID: rs201995154
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.12:4720746 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGACTCTGGCCATTGCTGTCAATCT[C/G]CTTCTGGTATTTTCTAGCAAGGGGA
Phenotype: MIM: 606250
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: GALNT8 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017417.1	161	Silent Mutation	CTC,CTG	L23L	NP_059113.1

There are no transcripts associated with this gene.