Product Details

SNP ID

rs9907259

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.17:35548265 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CAGTAGGCTGCCCTCTTTTCATAAA[A/G]CAGGTAGAGGTGTTTAATGGCTCTT

Phenotype

MIM: 614958

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SLFN14 PubMed Links

Gene Details

Gene

SLFN14

Gene Name

schlafen family member 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001129820.1	2833	Missense Mutation	CTT,TTT	L905F	NP_001123292.1
XM_017024576.1	2833	Missense Mutation	CTT,TTT	L905F	XP_016880065.1
XM_017024577.1	2833	Missense Mutation	CTT,TTT	L905F	XP_016880066.1
XM_017024578.1	2833	Missense Mutation	CTT,TTT	L905F	XP_016880067.1
XM_017024579.1	2833	Missense Mutation	CTT,TTT	L905F	XP_016880068.1

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