Product Details

SNP ID

rs1375862

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:122854758 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AAACACCTAATTCTGAGTTTCCCAT[A/G]GTTGTTAAATGGAGGGAAATGTTTT

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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