Product Details

SNP ID
rs201143062
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35352719 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCATTATTTGCTCCACAGTCAAGTA[C/T]TTCTTAATTCGTAAGGTTCCCTGAA
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 2678 Intron NP_001098057.1
NM_001104588.1 2678 Intron NP_001098058.1
NM_001104589.1 2678 Intron NP_001098059.1
NM_001104590.1 2678 Intron NP_001098060.1
NM_152270.3 2678 Intron NP_689483.3
XM_005258068.3 2678 Silent Mutation AAA,AAG K781K XP_005258125.1
XM_006722171.3 2678 Silent Mutation AAA,AAG K781K XP_006722234.1
XM_011525465.2 2678 Silent Mutation AAA,AAG K781K XP_011523767.1
XM_017025299.1 2678 Silent Mutation AAA,AAG K781K XP_016880788.1

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