Product Details

SNP ID
rs7211290
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35409711 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCACCTGGAGGCTTCATCAAAGTT[C/T]ACATTTTCTTTTGCTGATGTTTCAA
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 3632 Intron NP_001275938.1
NM_018042.4 3632 Intron NP_060512.3
XM_005257995.4 3632 UTR 3 XP_005258052.1
XM_011524967.2 3632 UTR 3 XP_011523269.1
XM_017024809.1 3632 UTR 3 XP_016880298.1
XM_017024810.1 3632 UTR 3 XP_016880299.1
XM_017024811.1 3632 Intron XP_016880300.1

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