Product Details

SNP ID
rs145662383
Assay Type
Functionally tested
NCBI dbSNP Submissions
12
Location
Chr.1:44410552 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGATGGTGTCCACTCATCTTCCCA[A/G]TTAATAACAGTCATTGACATGTCTG
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_001319956.1 199 Intron NP_001306885.1
NM_001319957.1 199 Intron NP_001306886.1
NM_018150.3 199 Intron NP_060620.2
XM_005270992.1 199 Intron XP_005271049.1
XM_005270993.1 199 Intron XP_005271050.1
XM_005270996.1 199 Intron XP_005271053.1
XM_006710735.3 199 Intron XP_006710798.1
XM_011541698.1 199 Intron XP_011540000.1
XM_011541699.1 199 Intron XP_011540001.1
XM_011541700.1 199 Intron XP_011540002.1
XM_011541702.1 199 Intron XP_011540004.1
XM_017001623.1 199 Intron XP_016857112.1
XM_017001624.1 199 UTR 5 XP_016857113.1
XM_017001625.1 199 Intron XP_016857114.1
XM_017001626.1 199 Intron XP_016857115.1

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