Product Details

SNP ID
rs200931762
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:29829603 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGGGGATGGAACCTTCCAGAAGTGG[A/G]CAGCTGTGGTGGTGCCTTCTGGAGA
Phenotype
MIM: 142871
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
HLA-G PubMed Links

Gene Details

Gene
HLA-G
Gene Name
major histocompatibility complex, class I, G
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_002127.5 538 Missense Mutation ACA,GCA T269A NP_002118.1
XM_017010816.1 538 Missense Mutation ACA,GCA T274A XP_016866305.1
XM_017010817.1 538 Missense Mutation ACA,GCA T177A XP_016866306.1
XM_017010818.1 538 Missense Mutation ACA,GCA T177A XP_016866307.1

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