Product Details

SNP ID
rs201333434
Assay Type
Functionally Tested
NCBI dbSNP Submissions
9
Location
Chr.1:40161601 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCTGAGGGAGCAAGAGGTGTCGGAG[A/G]TCTCATCTTTGAACTACTGCCGGAG
Phenotype
MIM: 180610
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
RLF PubMed Links

Gene Details

Gene
RLF
Gene Name
rearranged L-myc fusion
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_012421.3 233 Missense Mutation ATC,GTC I68V NP_036553.2
XM_017002016.1 233 UTR 5 XP_016857505.1
XM_017002017.1 233 UTR 5 XP_016857506.1
XM_017002018.1 233 UTR 5 XP_016857507.1

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