Product Details

SNP ID

rs56292880

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.6:29828622 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCTCCGCGGGTATGAACAGTATGC[C/G]TACGATGGCAAGGATTACCTCGCCC

Phenotype

MIM: 142871

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

HLA-G PubMed Links

Additional Information

For this assay, SNP(s) [rs1130356] 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-G

Gene Name

major histocompatibility complex, class I, G

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_002127.5	510	Silent Mutation	GCC,GCG	A141A	NP_002118.1
XM_017010816.1	510	Silent Mutation	GCC,GCG	A146A	XP_016866305.1
XM_017010817.1	510	Intron			XP_016866306.1
XM_017010818.1	510	Intron			XP_016866307.1

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