Product Details

SNP ID
rs12948161
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:35406748 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
AAAAACAAGTACAGTATGAAATCTT[C/G]CTTTTCAGTGAGCCAGTGAATTTTC
Phenotype
MIM: 614955
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SLFN12 PubMed Links

Gene Details

Gene
SLFN12
Gene Name
schlafen family member 12
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001289009.1 4722 Intron NP_001275938.1
NM_018042.4 4722 Intron NP_060512.3
XM_005257995.4 4722 UTR 3 XP_005258052.1
XM_011524967.2 4722 UTR 3 XP_011523269.1
XM_017024809.1 4722 UTR 3 XP_016880298.1
XM_017024810.1 4722 UTR 3 XP_016880299.1
XM_017024811.1 4722 Intron XP_016880300.1

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