Product Details

SNP ID
rs1350011
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35548370 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCAAACACGACAGTCCTCTCCAGGC[C/T]TGAAAATTGCTGAATACTGTCTAAA
Phenotype
MIM: 614958
Polymorphism
C/T, 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 2728 Missense Mutation AGC,GGC S870G NP_001123292.1
XM_017024576.1 2728 Missense Mutation AGC,GGC S870G XP_016880065.1
XM_017024577.1 2728 Missense Mutation AGC,GGC S870G XP_016880066.1
XM_017024578.1 2728 Missense Mutation AGC,GGC S870G XP_016880067.1
XM_017024579.1 2728 Missense Mutation AGC,GGC S870G XP_016880068.1

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