Product Details

SNP ID

rs2304968

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:35478131 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GAAGTTAATATATTCACGAAGAGGA[C/T]AACTCTGGGAGACAGGTGATGATGT

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	7899	Missense Mutation	TAT,TGT	Y383C	NP_001182719.1
XM_017024005.1	7899	Missense Mutation	TAT,TGT	Y412C	XP_016879494.1
XM_017024006.1	7899	Missense Mutation	TAT,TGT	Y383C	XP_016879495.1
XM_017024007.1	7899	Missense Mutation	TAT,TGT	Y383C	XP_016879496.1
XM_017024008.1	7899	Missense Mutation	TAT,TGT	Y365C	XP_016879497.1
XM_017024009.1	7899	Missense Mutation	TAT,TGT	Y365C	XP_016879498.1

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