Product Details

SNP ID: rs118151382
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:44699786 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TCCCTGACTTGTAGCCTCTCACTAA[C/T]TGCTGTCAACAAACCTGAAGTAGGG
Phenotype: MIM: 614591
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CEACAM16 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001039213.3		Intron			NP_001034302.2
XM_017026795.1		Intron			XP_016882284.1