Product Details

SNP ID

rs6088445

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:31516023 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCCCCAGGAGCAGAGAACTCACTA[C/T]TGGCTCTGTATGCGATCAGATGCAA

Phenotype

MIM: 607106

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

HM13 PubMed Links

Additional Information

For this assay, SNP(s) [rs75035893] 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

HM13

Gene Name

histocompatibility minor 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_030789.3		Intron			NP_110416.1
NM_178580.2		Intron			NP_848695.1
NM_178581.2		Intron			NP_848696.1
NM_178582.2		Intron			NP_848697.1

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