Product Details

SNP ID
rs11577388
Assay Type
Functionally Tested
NCBI dbSNP Submissions
47
Location
Chr.1:40162692 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AGTTAGCTTGCTTGATTGCTTTTCT[C/T]CCCTCTCTCTGCCGAGGCAGAAGCA
Phenotype
MIM: 180610
Polymorphism
C/T, 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 Intron NP_036553.2
XM_017002016.1 Intron XP_016857505.1
XM_017002017.1 Intron XP_016857506.1
XM_017002018.1 Intron XP_016857507.1

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