Product Details

SNP ID
hCV89768877
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.1:207322536 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACTCAGTGATCTGCCTTAAGGGCAG[G/T]CAATGGTCAGATATTGAAGAGTTCT
Phenotype
MIM: 125240
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
CD55 PubMed Links

Gene Details

Gene
CD55
Gene Name
CD55 molecule (Cromer blood group)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000574.4 549 Missense Mutation AGG,AGT R85S NP_000565.1
NM_001114752.2 549 Missense Mutation AGG,AGT R85S NP_001108224.1
NM_001300902.1 549 Missense Mutation AGG,AGT R85S NP_001287831.1
NM_001300903.1 549 Missense Mutation AGG,AGT R85S NP_001287832.1
NM_001300904.1 549 Missense Mutation AGG,AGT R85S NP_001287833.1

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