Product Details

SNP ID
rs55671218
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:58987920 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTTTTGGTGGCGGTGACAGACACTG[C/T]TCTTGACTCTAGGGGCCTATTAGGC
Phenotype
MIM: 605840
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
RNF111 PubMed Links

Gene Details

Gene
RNF111
Gene Name
ring finger protein 111
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001270528.1 295 UTR 5 NP_001257457.1
NM_001270529.1 295 UTR 5 NP_001257458.1
NM_001270530.1 295 Intron NP_001257459.1
NM_017610.7 295 UTR 5 NP_060080.6
XM_005254479.3 295 UTR 5 XP_005254536.1
XM_006720575.3 295 UTR 5 XP_006720638.1
XM_006720579.3 295 Intron XP_006720642.1
XM_011521694.2 295 Intron XP_011519996.2
XM_011521696.2 295 Intron XP_011519998.2
XM_011521697.2 295 Intron XP_011519999.2
XM_011521699.2 295 Intron XP_011520001.2
XM_017022336.1 295 UTR 5 XP_016877825.1
XM_017022337.1 295 UTR 5 XP_016877826.1
XM_017022338.1 295 UTR 5 XP_016877827.1
XM_017022339.1 295 UTR 5 XP_016877828.1
XM_017022340.1 295 UTR 5 XP_016877829.1
XM_017022341.1 295 Intron XP_016877830.1
XM_017022342.1 295 Intron XP_016877831.1
XM_017022343.1 295 Intron XP_016877832.1

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