Product Details

SNP ID

rs201703675

Assay Type

Functionally Tested

NCBI dbSNP Submissions

3

Location

Chr.1:25290685 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTGCTTTGTCGGTGCTGATCTCAG[C/T]GGATGCTGTCTTGGGGAAGGTCAAC

Phenotype

MIM: 111680

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RHD PubMed Links

Additional Information

For this assay, SNP(s) [rs542553378] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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	442	Missense Mutation	GCG,GTG	A127V	NP_001121163.1
NM_001282867.1	442	UTR 5			NP_001269796.1
NM_001282868.1	442	Missense Mutation	GCG,GTG	A127V	NP_001269797.1
NM_001282869.1	442	Missense Mutation	GCG,GTG	A127V	NP_001269798.1
NM_001282870.1	442	Missense Mutation	GCG,GTG	A127V	NP_001269799.1
NM_001282871.1	442	Missense Mutation	GCG,GTG	A127V	NP_001269800.1
NM_001282872.1	442	Missense Mutation	GCG,GTG	A127V	NP_001269801.1
NM_016124.4	442	Missense Mutation	GCG,GTG	A127V	NP_057208.2
XM_017002015.1	442	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	442	Intron			NP_001308701.1
NM_020317.4	442	Intron			NP_064713.3
XM_011541797.1	442	Intron			XP_011540099.1

View Full Product Details