Product Details

SNP ID
rs143462796
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35352680 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCTATCAAAGAAGCGCCTGCACGT[G/T]TCTGCCACACAGGTCATTATTTGCT
Phenotype
MIM: 614953
Polymorphism
G/T, Transversion 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 2717 Intron NP_001098057.1
NM_001104588.1 2717 Intron NP_001098058.1
NM_001104589.1 2717 Intron NP_001098059.1
NM_001104590.1 2717 Intron NP_001098060.1
NM_152270.3 2717 Intron NP_689483.3
XM_005258068.3 2717 Missense Mutation GAA,GAC E794D XP_005258125.1
XM_006722171.3 2717 Missense Mutation GAA,GAC E794D XP_006722234.1
XM_011525465.2 2717 Missense Mutation GAA,GAC E794D XP_011523767.1
XM_017025299.1 2717 Missense Mutation GAA,GAC E794D XP_016880788.1

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