Product Details

SNP ID

rs144978686

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:141742739 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTGTAGATCTGGCTCCACAGCCCTC[G/T]CTGTCCCCTCTGTCTCACTGGCTTC

Phenotype

MIM: 603863

Polymorphism

G/T, Transversion substitution

Allele Nomenclature

Literature Links

RNF7 PubMed Links

Gene Details

Gene

RNF7

Gene Name

ring finger protein 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001201370.1		Intron			NP_001188299.1
NM_014245.4		Intron			NP_055060.1
NM_183237.2		Intron			NP_899060.1

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