Product Details

SNP ID

rs10799479

Assay Type

Functionally tested

NCBI dbSNP Submissions

51

Location

Chr.1:228490809 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGAAGAGTGGCAAGTGTGAATGCT[A/G]TTTGTTGAAGGCTGATGGGATGGTT

Phenotype

MIM: 613754

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RNF187 PubMed Links

Gene Details

Gene

RNF187

Gene Name

ring finger protein 187

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001010858.2		Intron			NP_001010858.2

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