Product Details

SNP ID

rs28636630

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:31270261 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCCCCTCGTGCTGCATATGGCACG[G/T]GTATCTCTGCTCTTGTCCAGAAGGC

Phenotype

MIM: 142840

Polymorphism

G/T, Transversion Substitution

Allele Nomenclature

Literature Links

HLA-C PubMed Links

Additional Information

For this assay, SNP(s) [rs35424484] 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

HLA-C

Gene Name

major histocompatibility complex, class I, C

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001243042.1	909	Missense Mutation	ACG,CCG	T282P	NP_001229971.1
NM_002117.5	909	Missense Mutation	ACG,CCG	T282P	NP_002108.4

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