Product Details

SNP ID
rs184803752
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:37360553 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTTGAAGCAGAATCCTGAGGGCCA[A/G]TGGACAATTATGGACAACAAGGTAC
Phenotype
MIM: 611685
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RNF8 PubMed Links

Gene Details

Gene
RNF8
Gene Name
ring finger protein 8
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_003958.3 412 Silent Mutation CAA,CAG Q73Q NP_003949.1
NM_183078.2 412 Silent Mutation CAA,CAG Q73Q NP_898901.1
XM_006715241.2 412 Silent Mutation CAA,CAG Q73Q XP_006715304.1
XM_006715242.2 412 Silent Mutation CAA,CAG Q73Q XP_006715305.1
XM_017011462.1 412 Silent Mutation CAA,CAG Q16Q XP_016866951.1
XM_017011463.1 412 Silent Mutation CAA,CAG Q16Q XP_016866952.1
XM_017011464.1 412 UTR 5 XP_016866953.1

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