Product Details

SNP ID
rs188103921
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35479231 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTAGCAAACACTGCACAGCAGAAGC[A/G]TTCCACTCTGAGTGCATACACATAT
Phenotype
MIM: 614956
Polymorphism
A/G, 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 7730 Missense Mutation CGC,TGC R327C NP_001182719.1
XM_017024005.1 7730 Missense Mutation CGC,TGC R356C XP_016879494.1
XM_017024006.1 7730 Missense Mutation CGC,TGC R327C XP_016879495.1
XM_017024007.1 7730 Missense Mutation CGC,TGC R327C XP_016879496.1
XM_017024008.1 7730 Missense Mutation CGC,TGC R309C XP_016879497.1
XM_017024009.1 7730 Missense Mutation CGC,TGC R309C XP_016879498.1

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