Product Details

SNP ID
rs146142563
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:30491607 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCTGGTTCTCCTTGGATCTGTGGT[C/T]TCTGGAGCTGTGGTTGCTGCTGTGA
Phenotype
MIM: 143010
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
HLA-E PubMed Links

Gene Details

Gene
HLA-E
Gene Name
major histocompatibility complex, class I, E
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005516.5 1095 Silent Mutation GTC,GTT V319V NP_005507.3
XM_017010807.1 1095 Silent Mutation GTC,GTT V360V XP_016866296.1
XM_017010808.1 1095 Silent Mutation GTC,GTT V360V XP_016866297.1
XM_017010809.1 1095 Silent Mutation GTC,GTT V319V XP_016866298.1

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