Product Details

SNP ID
rs111955358
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35474969 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAACCAACAAACAAACAAACAAAAA[C/T]GAAACAAACAAACAAACAAAAAGAT
Phenotype
MIM: 614956
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLFN12L PubMed Links

Gene Details

Gene
SLFN12L
Gene Name
schlafen family member 12 like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001195790.1 8472 Missense Mutation CAT,CGT H574R NP_001182719.1
XM_017024005.1 8472 Missense Mutation CAT,CGT H603R XP_016879494.1
XM_017024006.1 8472 Missense Mutation CAT,CGT H574R XP_016879495.1
XM_017024007.1 8472 Missense Mutation CAT,CGT H574R XP_016879496.1
XM_017024008.1 8472 Missense Mutation CAT,CGT H556R XP_016879497.1
XM_017024009.1 8472 Missense Mutation CAT,CGT H556R XP_016879498.1

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