Product Details

SNP ID

hCV59935966

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:130873095 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ATGGGACACAGCCGGCCAGGAGAAA[C/T]TCGGTGGACTGAGAGATGGCTATTA

Phenotype

MIM: 601179

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

RAN PubMed Links

Gene Details

Gene

RAN

Gene Name

RAN, member RAS oncogene family

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001300796.1	303	UTR 5			NP_001287725.1
NM_001300797.1	303	UTR 5			NP_001287726.1
NM_006325.4	303	Missense Mutation	CTC,TTC	L72F	NP_006316.1

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