Product Details

SNP ID
rs142904530
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:25290689 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTTGTCGGTGCTGATCTCAGTGGA[C/T]GCTGTCTTGGGGAAGGTCAACTTGG
Phenotype
MIM: 111680
Polymorphism
C/T, Transition 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_001127691.2 446 Silent Mutation GAC,GAT D128D NP_001121163.1
NM_001282867.1 446 UTR 5 NP_001269796.1
NM_001282868.1 446 Silent Mutation GAC,GAT D128D NP_001269797.1
NM_001282869.1 446 Silent Mutation GAC,GAT D128D NP_001269798.1
NM_001282870.1 446 Silent Mutation GAC,GAT D128D NP_001269799.1
NM_001282871.1 446 Silent Mutation GAC,GAT D128D NP_001269800.1
NM_001282872.1 446 Silent Mutation GAC,GAT D128D NP_001269801.1
NM_016124.4 446 Silent Mutation GAC,GAT D128D NP_057208.2
XM_017002015.1 446 Intron XP_016857504.1
Gene
RSRP1
Gene Name
arginine and serine rich protein 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001321772.1 446 Intron NP_001308701.1
NM_020317.4 446 Intron NP_064713.3
XM_011541797.1 446 Intron XP_011540099.1

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