Product Details

SNP ID

rs3744372

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:35475137 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GCTTGTCTTGCCTTCAGGGCTCAAG[G/T]AGAAGATCTTTGTCATGACACACAC

Phenotype

MIM: 614956

Polymorphism

G/T, Transversion 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	8304	Missense Mutation	TAC,TCC	Y518S	NP_001182719.1
XM_017024005.1	8304	Missense Mutation	TAC,TCC	Y547S	XP_016879494.1
XM_017024006.1	8304	Missense Mutation	TAC,TCC	Y518S	XP_016879495.1
XM_017024007.1	8304	Missense Mutation	TAC,TCC	Y518S	XP_016879496.1
XM_017024008.1	8304	Missense Mutation	TAC,TCC	Y500S	XP_016879497.1
XM_017024009.1	8304	Missense Mutation	TAC,TCC	Y500S	XP_016879498.1

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