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SNP ID
rs76039941
Assay Type
Functionally tested
NCBI dbSNP Submissions
11
Location
Chr.1:51251556 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCATTTTTTGAAATATCAAAAAATT[A/G]AGGTATGTCATGATGGATGCATAAA
Phenotype
MIM: 612598
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RNF11 PubMed Links

Gene Details

Gene
RNF11
Gene Name
ring finger protein 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_014372.4 Intron NP_055187.1

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