Product Details

SNP ID
rs201843188
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:30492573 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGTGCCCAGGGGTCTGAGTCTCAC[A/C]GCTTGTAAAGGTGAGATTCTGGGGG
Phenotype
MIM: 143010
Polymorphism
A/C, Transversion 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 1207 Missense Mutation AGC,CGC S357R NP_005507.3
XM_017010807.1 1207 Missense Mutation AGC,CGC S398R XP_016866296.1
XM_017010808.1 1207 Missense Mutation AGC,CGC S398R XP_016866297.1
XM_017010809.1 1207 UTR 3 XP_016866298.1

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