Product Details

SNP ID
rs200176335
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:130874641 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGATCTGGTACGAGTGTGTGAAAAC[A/G]TCCCCATTGTGTTGTGTGGCAACAA
Phenotype
MIM: 601179
Polymorphism
A/G, 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_001300796.1 432 Missense Mutation ATC,GTC I27V NP_001287725.1
NM_001300797.1 432 Missense Mutation ATC,GTC I27V NP_001287726.1
NM_006325.4 432 Missense Mutation ATC,GTC I115V NP_006316.1
XM_017019772.1 432 Missense Mutation ATC,GTC I115V XP_016875261.1
XM_017019773.1 432 Missense Mutation ATC,GTC I27V XP_016875262.1

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