Product Details

SNP ID
rs201522161
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:41336139 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TACTTCAAAGTGTGGCAGGGCAGAC[A/G]CTAACCGTGAGATGCCAGTACCCGC
Phenotype
MIM: 604531
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
NCR2 PubMed Links

Gene Details

Gene
NCR2
Gene Name
natural cytotoxicity triggering receptor 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001199509.1 192 Silent Mutation ACA,ACG T35T NP_001186438.1
NM_001199510.1 192 Silent Mutation ACA,ACG T35T NP_001186439.1
NM_004828.3 192 Silent Mutation ACA,ACG T35T NP_004819.2
XM_017011500.1 192 Silent Mutation ACA,ACG T43T XP_016866989.1

View Full Product Details