Product Details

SNP ID
rs200212435
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:124488631 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AAAAAATACTTTAATAGTATTGTTA[C/T]ATAGTGTATTGGCTAATTCCAGTGG
Phenotype
MIM: 603046
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RNF139 PubMed Links

Gene Details

Gene
RNF139
Gene Name
ring finger protein 139
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_007218.3 783 Intron NP_009149.2
XM_017013002.1 783 Intron XP_016868491.1
Gene
TATDN1
Gene Name
TatD DNase domain containing 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001146160.1 783 Missense Mutation TAT,TGT Y239C NP_001139632.1
NM_001317889.1 783 Missense Mutation TAT,TGT Y322C NP_001304818.1
NM_001317890.1 783 Missense Mutation TAT,TGT Y232C NP_001304819.1
NM_001317891.1 783 Missense Mutation TAT,TGT Y141C NP_001304820.1
NM_032026.3 783 Missense Mutation TAT,TGT Y286C NP_114415.1
XM_006716666.3 783 Intron XP_006716729.1
XM_006716667.3 783 Intron XP_006716730.1
XM_006716668.3 783 Intron XP_006716731.1
XM_006716669.3 783 Intron XP_006716732.1
XM_006716670.3 783 Intron XP_006716733.1
XM_006716671.3 783 Intron XP_006716734.1
XM_011517331.2 783 Intron XP_011515633.1
XM_017013895.1 783 Intron XP_016869384.1
XM_017013896.1 783 Intron XP_016869385.1
XM_017013897.1 783 Intron XP_016869386.1
XM_017013898.1 783 Intron XP_016869387.1
XM_017013899.1 783 Intron XP_016869388.1

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