Product Details

SNP ID

rs111747661

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.20:31514503 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGAGCCGGTGTCTCCGCCTGCGTC[C/T]CTGCTGCAGCAACCGGAGCTGGAGT

Phenotype

MIM: 607106

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

HM13 PubMed Links

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	94	UTR 5			NP_110416.1
NM_178580.2	94	UTR 5			NP_848695.1
NM_178581.2	94	UTR 5			NP_848696.1
NM_178582.2	94	UTR 5			NP_848697.1

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