Product Details

SNP ID

rs10933936

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.3:108302447 on Build GRCh38

Set Membership

Validated

Context Sequence [VIC/FAM]

TTGCATTTTGATTGGTTCAAATTCC[A/G]TGTGGGGATTCCTTGATTCTGACAG

Phenotype

MIM: 604371

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

HHLA2 PubMed Links

Additional Information

For this assay, SNP(s) [rs74409632] 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

HHLA2

Gene Name

HERV-H LTR-associating 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001282556.1		Intron			NP_001269485.1
NM_001282557.1		Intron			NP_001269486.1
NM_001282558.1		Intron			NP_001269487.1
NM_001282559.1		Intron			NP_001269488.1
NM_007072.3		Intron			NP_009003.1
XM_005247080.3		Intron			XP_005247137.1
XM_011512362.1		Intron			XP_011510664.1
XM_011512363.1		Intron			XP_011510665.1
XM_011512364.1		Intron			XP_011510666.1
XM_011512367.2		Intron			XP_011510669.1
XM_017005642.1		Intron			XP_016861131.1

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