Product Details

SNP ID
rs184079642
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35352746 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTTAATTCGTAAGGTTCCCTGAAC[A/G]CCCTGGGACCATTCGGCTTCAGGAA
Phenotype
MIM: 614953
Polymorphism
A/G, 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 2651 Intron NP_001098057.1
NM_001104588.1 2651 Intron NP_001098058.1
NM_001104589.1 2651 Intron NP_001098059.1
NM_001104590.1 2651 Intron NP_001098060.1
NM_152270.3 2651 Intron NP_689483.3
XM_005258068.3 2651 Silent Mutation GGC,GGT G772G XP_005258125.1
XM_006722171.3 2651 Silent Mutation GGC,GGT G772G XP_006722234.1
XM_011525465.2 2651 Silent Mutation GGC,GGT G772G XP_011523767.1
XM_017025299.1 2651 Silent Mutation GGC,GGT G772G XP_016880788.1

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