Product Details

SNP ID
rs1130356
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:29828550 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CCGAGGGGGTGGGGCCAGGTTCTCA[C/T]ACCCTCCAGTGGATGATTGGCTGCG
Phenotype
MIM: 142871
Polymorphism
C/T, 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_002127.5 438 Silent Mutation CAC,CAT H117H NP_002118.1
XM_017010816.1 438 Silent Mutation CAC,CAT H122H XP_016866305.1
XM_017010817.1 438 Intron XP_016866306.1
XM_017010818.1 438 Intron XP_016866307.1

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