Product Details

SNP ID
rs149052916
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35352881 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GATCTGCATTGCGAACTATTCTGGT[A/G]AGCTCTTCTCTTGGATATTGGTCTG
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 2516 Intron NP_001098057.1
NM_001104588.1 2516 Intron NP_001098058.1
NM_001104589.1 2516 Intron NP_001098059.1
NM_001104590.1 2516 Intron NP_001098060.1
NM_152270.3 2516 Intron NP_689483.3
XM_005258068.3 2516 Silent Mutation CTC,CTT L727L XP_005258125.1
XM_006722171.3 2516 Silent Mutation CTC,CTT L727L XP_006722234.1
XM_011525465.2 2516 Silent Mutation CTC,CTT L727L XP_011523767.1
XM_017025299.1 2516 Silent Mutation CTC,CTT L727L XP_016880788.1

View Full Product Details