Product Details

SNP ID

rs7683365

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:143999443 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGTGAAACGATGGACAAGTTGTCCC[A/G]TTTCTCCTATAAAGCAAAATTTCAA

Phenotype

MIM: 111740

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

GYPB PubMed Links

Additional Information

For this assay, SNP(s) [rs7662277] 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	201	Missense Mutation	ACG,ATG	T22M	NP_001291311.1
NM_002100.5	201	Missense Mutation	ACG,ATG	T48M	NP_002091.3
XM_011531903.2	201	Missense Mutation	ACG,ATG	T48M	XP_011530205.1
XM_011531904.2	201	Intron			XP_011530206.1
XM_011531905.2	201	Missense Mutation	ACG,ATG	T39M	XP_011530207.1
XM_017008137.1	201	Missense Mutation	ACG,ATG	T22M	XP_016863626.1

View Full Product Details