Product Details

SNP ID

rs17106462

Assay Type

Functionally tested

NCBI dbSNP Submissions

18

Location

Chr.1:51245843 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTAAGGAAGGTAATACATAAAAGAC[A/G]TATTTGCAAACGACTTGAGGCAAGA

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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