Product Details

SNP ID
rs3905017
Assay Type
Functionally tested
NCBI dbSNP Submissions
11
Location
Chr.1:44406957 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAGTCCCGAAGTAGCGGGGACTAG[A/G]GCAGCCAGGAGGCAGGGGGAAAGCT
Phenotype
MIM: 616136
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
RNF220 PubMed Links

Gene Details

Gene
RNF220
Gene Name
ring finger protein 220
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001319956.1 196 Intron NP_001306885.1
NM_001319957.1 196 Intron NP_001306886.1
NM_018150.3 196 Intron NP_060620.2
XM_005270992.1 196 Intron XP_005271049.1
XM_005270993.1 196 Intron XP_005271050.1
XM_005270996.1 196 Intron XP_005271053.1
XM_006710735.3 196 Intron XP_006710798.1
XM_011541698.1 196 Intron XP_011540000.1
XM_011541699.1 196 UTR 5 XP_011540001.1
XM_011541700.1 196 Intron XP_011540002.1
XM_011541702.1 196 Intron XP_011540004.1
XM_017001623.1 196 UTR 5 XP_016857112.1
XM_017001624.1 196 Intron XP_016857113.1
XM_017001625.1 196 Intron XP_016857114.1
XM_017001626.1 196 Intron XP_016857115.1

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