Product Details

SNP ID: rs2199829
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.19:41809519 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: GAGAGAGAGGACAAGGACACTGTCC[C/T]ATTTCAGCATCACCAGCCCTGAGTG
Phenotype: MIM: 609142
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CEACAM3 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001277163.2		Intron			NP_001264092.1
NM_001815.4		Intron			NP_001806.2