Product Details

SNP ID

rs142064832

Assay Type

Functionally tested

NCBI dbSNP Submissions

7

Location

Chr.1:19076837 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGCAGCTTCGTAGATGGGCATGTC[A/G]TTGTGGCGGATGTACTCAGCGAGAG

Phenotype

MIM: 609890

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

UBR4 PubMed Links

Gene Details

Gene

UBR4

Gene Name

ubiquitin protein ligase E3 component n-recognin 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020765.2	15371	Silent Mutation	AAC,AAT	N5130N	NP_065816.2
XM_011541108.2	15371	Silent Mutation	AAC,AAT	N5181N	XP_011539410.1
XM_011541109.2	15371	Silent Mutation	AAC,AAT	N5180N	XP_011539411.1
XM_011541110.2	15371	Silent Mutation	AAC,AAT	N5180N	XP_011539412.1
XM_011541111.2	15371	Silent Mutation	AAC,AAT	N5180N	XP_011539413.1
XM_011541112.2	15371	Silent Mutation	AAC,AAT	N5176N	XP_011539414.1
XM_011541113.2	15371	Silent Mutation	AAC,AAT	N5175N	XP_011539415.1
XM_011541114.2	15371	Silent Mutation	AAC,AAT	N5175N	XP_011539416.1
XM_011541115.2	15371	Silent Mutation	AAC,AAT	N5173N	XP_011539417.1
XM_011541116.2	15371	Silent Mutation	AAC,AAT	N5170N	XP_011539418.1
XM_011541117.2	15371	Silent Mutation	AAC,AAT	N5153N	XP_011539419.1
XM_011541118.2	15371	Silent Mutation	AAC,AAT	N5152N	XP_011539420.1
XM_011541119.2	15371	Silent Mutation	AAC,AAT	N5141N	XP_011539421.1
XM_011541120.2	15371	Silent Mutation	AAC,AAT	N5140N	XP_011539422.1
XM_011541121.2	15371	Silent Mutation	AAC,AAT	N5129N	XP_011539423.1
XM_017000822.1	15371	Silent Mutation	AAC,AAT	N5174N	XP_016856311.1
XM_017000823.1	15371	Silent Mutation	AAC,AAT	N5165N	XP_016856312.1
XM_017000824.1	15371	Silent Mutation	AAC,AAT	N5147N	XP_016856313.1
XM_017000825.1	15371	Silent Mutation	AAC,AAT	N5142N	XP_016856314.1
XM_017000826.1	15371	Silent Mutation	AAC,AAT	N5141N	XP_016856315.1
XM_017000827.1	15371	Silent Mutation	AAC,AAT	N5136N	XP_016856316.1
XM_017000828.1	15371	Silent Mutation	AAC,AAT	N5128N	XP_016856317.1
XM_017000829.1	15371	Silent Mutation	AAC,AAT	N5112N	XP_016856318.1
XM_017000830.1	15371	Silent Mutation	AAC,AAT	N5095N	XP_016856319.1

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