Product Details

SNP ID
rs142470821
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35352709 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCCACACAGGTCATTATTTGCTCCA[A/C]AGTCAAGTATTTCTTAATTCGTAAG
Phenotype
MIM: 614953
Polymorphism
A/C, 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 2688 Intron NP_001098057.1
NM_001104588.1 2688 Intron NP_001098058.1
NM_001104589.1 2688 Intron NP_001098059.1
NM_001104590.1 2688 Intron NP_001098060.1
NM_152270.3 2688 Intron NP_689483.3
XM_005258068.3 2688 Missense Mutation GTG,TTG V785L XP_005258125.1
XM_006722171.3 2688 Missense Mutation GTG,TTG V785L XP_006722234.1
XM_011525465.2 2688 Missense Mutation GTG,TTG V785L XP_011523767.1
XM_017025299.1 2688 Missense Mutation GTG,TTG V785L XP_016880788.1

View Full Product Details