Product Details

SNP ID

rs112342416

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:44412124 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGACTTACACCGGGCAGCCTTCAA[A/G]ATGGAGAACTCATCCTACCTTCCCA

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	683	Silent Mutation	AAA,AAG	K9K	NP_001306885.1
NM_001319957.1	683	Intron			NP_001306886.1
NM_018150.3	683	Silent Mutation	AAA,AAG	K9K	NP_060620.2
XM_005270992.1	683	Silent Mutation	AAA,AAG	K9K	XP_005271049.1
XM_005270993.1	683	Silent Mutation	AAA,AAG	K9K	XP_005271050.1
XM_005270996.1	683	Intron			XP_005271053.1
XM_006710735.3	683	Silent Mutation	AAA,AAG	K9K	XP_006710798.1
XM_011541698.1	683	Silent Mutation	AAA,AAG	K9K	XP_011540000.1
XM_011541699.1	683	Silent Mutation	AAA,AAG	K9K	XP_011540001.1
XM_011541700.1	683	Silent Mutation	AAA,AAG	K9K	XP_011540002.1
XM_011541702.1	683	Intron			XP_011540004.1
XM_017001623.1	683	Silent Mutation	AAA,AAG	K9K	XP_016857112.1
XM_017001624.1	683	Silent Mutation	AAA,AAG	K9K	XP_016857113.1
XM_017001625.1	683	Silent Mutation	AAA,AAG	K9K	XP_016857114.1
XM_017001626.1	683	Intron			XP_016857115.1

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