Product Details

SNP ID
rs11546819
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:31514701 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGGCGCTGCTGCCCATCTTCTTCGG[C/T]GCCCTGCGCTCCGTACGCTGCGCCC
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_030789.3 292 Silent Mutation GGC,GGT G50G NP_110416.1
NM_178580.2 292 Silent Mutation GGC,GGT G50G NP_848695.1
NM_178581.2 292 Silent Mutation GGC,GGT G50G NP_848696.1
NM_178582.2 292 Silent Mutation GGC,GGT G50G NP_848697.1

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