Product Details

SNP ID
rs199944678
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35352730 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCACAGTCAAGTATTTCTTAATTC[G/T]TAAGGTTCCCTGAACACCCTGGGAC
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 2667 Intron NP_001098057.1
NM_001104588.1 2667 Intron NP_001098058.1
NM_001104589.1 2667 Intron NP_001098059.1
NM_001104590.1 2667 Intron NP_001098060.1
NM_152270.3 2667 Intron NP_689483.3
XM_005258068.3 2667 Nonsense Mutation XP_005258125.1
XM_006722171.3 2667 Nonsense Mutation XP_006722234.1
XM_011525465.2 2667 Nonsense Mutation XP_011523767.1
XM_017025299.1 2667 Nonsense Mutation XP_016880788.1

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