Product Details

SNP ID
rs3866647
Assay Type
Functionally tested
NCBI dbSNP Submissions
17
Location
Chr.1:44411154 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTAGTAACTAAAATCACCGATCTGT[C/T]CTTTGCTGCCCTTAGAAGACAGATG
Phenotype
MIM: 616136
Polymorphism
C/T, 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 Intron NP_001306885.1
NM_001319957.1 Intron NP_001306886.1
NM_018150.3 Intron NP_060620.2
XM_005270992.1 Intron XP_005271049.1
XM_005270993.1 Intron XP_005271050.1
XM_005270996.1 Intron XP_005271053.1
XM_006710735.3 Intron XP_006710798.1
XM_011541698.1 Intron XP_011540000.1
XM_011541699.1 Intron XP_011540001.1
XM_011541700.1 Intron XP_011540002.1
XM_011541702.1 Intron XP_011540004.1
XM_017001623.1 Intron XP_016857112.1
XM_017001624.1 Intron XP_016857113.1
XM_017001625.1 Intron XP_016857114.1
XM_017001626.1 Intron XP_016857115.1

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