Product Details

SNP ID
rs147143249
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35352682 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTATCAAAGAAGCGCCTGCACGTGT[C/T]TGCCACACAGGTCATTATTTGCTCC
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 2715 Intron NP_001098057.1
NM_001104588.1 2715 Intron NP_001098058.1
NM_001104589.1 2715 Intron NP_001098059.1
NM_001104590.1 2715 Intron NP_001098060.1
NM_152270.3 2715 Intron NP_689483.3
XM_005258068.3 2715 Missense Mutation AAC,GAC N794D XP_005258125.1
XM_006722171.3 2715 Missense Mutation AAC,GAC N794D XP_006722234.1
XM_011525465.2 2715 Missense Mutation AAC,GAC N794D XP_011523767.1
XM_017025299.1 2715 Missense Mutation AAC,GAC N794D XP_016880788.1

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