Product Details

SNP ID
rs78617576
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.15:58990090 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTATCTTATGAAATAATATAGGGCT[A/G]AGGACAGGAGATCTAGATTTTAGAT
Phenotype
MIM: 605840
Polymorphism
A/G, 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 Intron NP_001257457.1
NM_001270529.1 Intron NP_001257458.1
NM_001270530.1 Intron NP_001257459.1
NM_017610.7 Intron NP_060080.6
XM_005254479.3 Intron XP_005254536.1
XM_006720575.3 Intron XP_006720638.1
XM_006720579.3 Intron XP_006720642.1
XM_011521694.2 Intron XP_011519996.2
XM_011521696.2 Intron XP_011519998.2
XM_011521697.2 Intron XP_011519999.2
XM_011521699.2 Intron XP_011520001.2
XM_017022336.1 Intron XP_016877825.1
XM_017022337.1 Intron XP_016877826.1
XM_017022338.1 Intron XP_016877827.1
XM_017022339.1 Intron XP_016877828.1
XM_017022340.1 Intron XP_016877829.1
XM_017022341.1 Intron XP_016877830.1
XM_017022342.1 Intron XP_016877831.1
XM_017022343.1 Intron XP_016877832.1

View Full Product Details