Product Details

SNP ID
rs192840240
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35352685 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCAAAGAAGCGCCTGCACGTGTCTG[C/T]CACACAGGTCATTATTTGCTCCACA
Phenotype
MIM: 614953
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLFN11 PubMed Links

Gene Details

Gene
SLFN11
Gene Name
schlafen family member 11
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001104587.1 2712 Intron NP_001098057.1
NM_001104588.1 2712 Intron NP_001098058.1
NM_001104589.1 2712 Intron NP_001098059.1
NM_001104590.1 2712 Intron NP_001098060.1
NM_152270.3 2712 Intron NP_689483.3
XM_005258068.3 2712 Missense Mutation ACA,GCA T793A XP_005258125.1
XM_006722171.3 2712 Missense Mutation ACA,GCA T793A XP_006722234.1
XM_011525465.2 2712 Missense Mutation ACA,GCA T793A XP_011523767.1
XM_017025299.1 2712 Missense Mutation ACA,GCA T793A XP_016880788.1

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