Product Details

SNP ID

rs147012546

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:122856100 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTTTGTCCTTTAAGTGCTCATATG[A/G]AACATTTGACTAATACTATCAAAAC

Phenotype

MIM: 615231

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

RC3H2 PubMed Links

Gene Details

Gene

RC3H2

Gene Name

ring finger and CCCH-type domains 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001100588.1		Intron			NP_001094058.1
NM_018835.2		Intron			NP_061323.2

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