Product Details

SNP ID
rs199819830
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.4:143997607 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCAATAATACCAGCCATCACACAC[A/C]AAATAATGAGTATTATCACTACAGG
Phenotype
MIM: 111740
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
GYPB PubMed Links
Additional Information
For this assay, SNP(s) [rs1132783] 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
GYPB
Gene Name
glycophorin B (MNS blood group)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001304382.1 261 Missense Mutation TGG,TTG W42L NP_001291311.1
NM_002100.5 261 Missense Mutation TGG,TTG W68L NP_002091.3
XM_011531903.2 261 Missense Mutation TGG,TTG W68L XP_011530205.1
XM_011531904.2 261 Intron XP_011530206.1
XM_011531905.2 261 Missense Mutation TGG,TTG W59L XP_011530207.1
XM_017008137.1 261 Missense Mutation TGG,TTG W42L XP_016863626.1

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