Product Details

SNP ID
rs11751749
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:37354118 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GATGCACAGAGGCAGCCAGAACCTA[G/T]GTCAGGGTCTCGCTCGGTGCTGACC
Phenotype
MIM: 611685
Polymorphism
G/T, Transversion 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_003958.3 147 UTR 5 NP_003949.1
NM_183078.2 147 UTR 5 NP_898901.1
XM_006715241.2 147 UTR 5 XP_006715304.1
XM_006715242.2 147 UTR 5 XP_006715305.1
XM_017011462.1 147 Intron XP_016866951.1
XM_017011463.1 147 Intron XP_016866952.1
XM_017011464.1 147 UTR 5 XP_016866953.1

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