Product Details

SNP ID
rs73559882
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:43360267 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACCCTGGGATTCCTCTCCCCAGAT[G/T]TTCTGACCTGTCATCGGGGGACCAC
Phenotype
MIM: 162860
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
CD177 PubMed Links

Gene Details

Gene
CD177
Gene Name
CD177 molecule
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_020406.3 678 Missense Mutation GTT,TTT V208F NP_065139.2
XM_017027021.1 678 Missense Mutation GTT,TTT V208F XP_016882510.1
XM_017027022.1 678 Missense Mutation GTT,TTT V208F XP_016882511.1

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