Product Details

SNP ID
rs80310291
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35475045 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAAGGGCCTTTTCCAAGTCTTTCA[C/T]TGTTTGAGCTGTTGTCCAATAGTAG
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 8396 Missense Mutation ATG,GTG M549V NP_001182719.1
XM_017024005.1 8396 Missense Mutation ATG,GTG M578V XP_016879494.1
XM_017024006.1 8396 Missense Mutation ATG,GTG M549V XP_016879495.1
XM_017024007.1 8396 Missense Mutation ATG,GTG M549V XP_016879496.1
XM_017024008.1 8396 Missense Mutation ATG,GTG M531V XP_016879497.1
XM_017024009.1 8396 Missense Mutation ATG,GTG M531V XP_016879498.1

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