Product Details

SNP ID

rs17850027

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:141738455 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCTCCCTCAAGAAGTGGAACGCGGT[C/G]GCCATGTGGAGCTGGGACGTGGAGT

Phenotype

MIM: 603863

Polymorphism

C/G, 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	247	Silent Mutation	GTC,GTG	V38V	NP_001188299.1
NM_014245.4	247	Silent Mutation	GTC,GTG	V38V	NP_055060.1
NM_183237.2	247	Silent Mutation	GTC,GTG	V38V	NP_899060.1

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