Product Details

SNP ID

rs146151828

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:51236771 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGCTCCGGAAGATGGGGAACTGCCT[C/G]AAATCCCCCACCTCGGATGACATCT

Phenotype

MIM: 612598

Polymorphism

C/G, Transversion 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	499	Silent Mutation	CTC,CTG	L5L	NP_055187.1

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