Product Details

SNP ID
rs2681072
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35407398 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTCTTATATTAGCCCCTGGATATAA[C/T]ATTAATGTACCAAACTTCCGGCAAA
Phenotype
MIM: 614955
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLFN12 PubMed Links

Gene Details

Gene
SLFN12
Gene Name
schlafen family member 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001289009.1 4072 Intron NP_001275938.1
NM_018042.4 4072 Intron NP_060512.3
XM_005257995.4 4072 UTR 3 XP_005258052.1
XM_011524967.2 4072 UTR 3 XP_011523269.1
XM_017024809.1 4072 UTR 3 XP_016880298.1
XM_017024810.1 4072 UTR 3 XP_016880299.1
XM_017024811.1 4072 Intron XP_016880300.1

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