Product Details

SNP ID
hCV57665659
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.1:25313000 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATTTTGCATGTAAGAAGGACATGC[A/T]TTTTGGGGGCTGGGGCAGGATGCTG
Phenotype
MIM: 111680
Polymorphism
A/T, Transversion Substitution
Allele Nomenclature
Literature Links
RHD PubMed Links

Gene Details

Gene
RHD
Gene Name
Rh blood group D antigen
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001127691.2 Intron NP_001121163.1
NM_001282867.1 Intron NP_001269796.1
NM_001282868.1 Intron NP_001269797.1
NM_001282869.1 Intron NP_001269798.1
NM_001282870.1 Intron NP_001269799.1
NM_001282871.1 Intron NP_001269800.1
NM_001282872.1 Intron NP_001269801.1
NM_016124.4 Intron NP_057208.2
Gene
RSRP1
Gene Name
arginine and serine rich protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321772.1 Intron NP_001308701.1
NM_020317.4 Intron NP_064713.3

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