Product Details

SNP ID

rs145535549

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.3:141738449 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGATGTTCTCCCTCAAGAAGTGGAA[C/T]GCGGTGGCCATGTGGAGCTGGGACG

Phenotype

MIM: 603863

Polymorphism

C/T, Transition 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	241	Silent Mutation	AAC,AAT	N36N	NP_001188299.1
NM_014245.4	241	Silent Mutation	AAC,AAT	N36N	NP_055060.1
NM_183237.2	241	Silent Mutation	AAC,AAT	N36N	NP_899060.1

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