Product Details

SNP ID
rs201983898
Assay Type
Functionally tested
NCBI dbSNP Submissions
3
Location
Chr.1:40161486 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TAGCGGGAGCCGGAGATGGAGTCGA[C/G]ACTGAGTCCATGGTTCGGGGTCATC
Phenotype
MIM: 180610
Polymorphism
C/G, Transversion 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_012421.3 118 Missense Mutation GAC,GAG D29E NP_036553.2
XM_017002016.1 118 UTR 5 XP_016857505.1
XM_017002017.1 118 UTR 5 XP_016857506.1
XM_017002018.1 118 UTR 5 XP_016857507.1

View Full Product Details