Product Details

SNP ID

rs144163296

Assay Type

Functionally Tested

NCBI dbSNP Submissions

9

Location

Chr.1:25390838 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTAGAGCATAGTAGGTGTTGAACA[C/T]GGCATTCTTCCTTTGGATTGGACTT

Phenotype

MIM: 111700

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

RHCE PubMed Links

Additional Information

For this assay, SNP(s) [rs1053361] 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

RHCE

Gene Name

Rh blood group CcEe antigens

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020485.4	798	Missense Mutation	ATG,GTG	M238V	NP_065231.3
NM_138616.3	798	Intron			NP_619522.3
NM_138617.3	798	Intron			NP_619523.3
NM_138618.3	798	Missense Mutation	ATG,GTG	M238V	NP_619524.3
XM_005245957.3	798	Missense Mutation	ATG,GTG	M238V	XP_005246014.1
XM_006710810.3	798	Intron			XP_006710873.1
XM_011541888.2	798	Missense Mutation	ATG,GTG	M198V	XP_011540190.1
XM_011541889.2	798	Missense Mutation	ATG,GTG	M195V	XP_011540191.1
XM_011541890.2	798	Missense Mutation	ATG,GTG	M238V	XP_011540192.1
XM_011541891.2	798	Missense Mutation	ATG,GTG	M182V	XP_011540193.1
XM_017002014.1	798	Missense Mutation	ATG,GTG	M238V	XP_016857503.1

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