Product Details

SNP ID
rs34345974
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:41336093 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTACTTCATCATTCTCCAGGCTCTC[A/G]GGCACAATCCAAGGCTCAGGTACTT
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_001199509.1 146 Missense Mutation CAG,CGG Q20R NP_001186438.1
NM_001199510.1 146 Missense Mutation CAG,CGG Q20R NP_001186439.1
NM_004828.3 146 Missense Mutation CAG,CGG Q20R NP_004819.2
XM_017011500.1 146 Missense Mutation CAG,CGG Q28R XP_016866989.1

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