Product Details

SNP ID

rs143749704

Assay Type

Functionally tested

NCBI dbSNP Submissions

6

Location

Chr.1:44412619 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGACACAGCTGCCATCTAGCTCCCC[C/T]GGTTCACTAAAGGTTGATGACACTG

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	1178	Silent Mutation	CCC,CCT	P174P	NP_001306885.1
NM_001319957.1	1178	Intron			NP_001306886.1
NM_018150.3	1178	Silent Mutation	CCC,CCT	P174P	NP_060620.2
XM_005270992.1	1178	Silent Mutation	CCC,CCT	P174P	XP_005271049.1
XM_005270993.1	1178	Silent Mutation	CCC,CCT	P174P	XP_005271050.1
XM_005270996.1	1178	Intron			XP_005271053.1
XM_006710735.3	1178	Silent Mutation	CCC,CCT	P174P	XP_006710798.1
XM_011541698.1	1178	Silent Mutation	CCC,CCT	P174P	XP_011540000.1
XM_011541699.1	1178	Silent Mutation	CCC,CCT	P174P	XP_011540001.1
XM_011541700.1	1178	Silent Mutation	CCC,CCT	P174P	XP_011540002.1
XM_011541702.1	1178	Intron			XP_011540004.1
XM_017001623.1	1178	Silent Mutation	CCC,CCT	P174P	XP_016857112.1
XM_017001624.1	1178	Silent Mutation	CCC,CCT	P174P	XP_016857113.1
XM_017001625.1	1178	Silent Mutation	CCC,CCT	P174P	XP_016857114.1
XM_017001626.1	1178	Intron			XP_016857115.1

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