chr2:73938891:C>T Detail (hg38) (DGUOK)

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Summary
Information
Links
Disease area statistics
MGeND
ClinVar
CIViC
DisGeNET
Annotation
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Information

Genome

Assembly	Position
hg19	chr2:74,166,018-74,166,018 View the variant detail on this assembly version.
hg38	chr2:73,938,891-73,938,891

HGVS

DGUOK

Type	Transcript	Protein
RefSeq	NM_001318860.1:c.143-19C>T
	NM_001318861.1:c.143-19C>T
	NM_001318862.1:c.143-19C>T
	NM_001318863.1:c.143-19C>T
	NM_080916.2:c.143-19C>T
	NM_001318859.1:c.143-19C>T
	NM_080918.2:c.143-19C>T
	NR_134894.1:c.143-7828C>T
	NR_134898.1:c.143-7828C>T
Ensemble	ENST00000264093.9:c.143-19C>T
	ENST00000348222.3:c.143-19C>T
	ENST00000629438.2:c.143-7828C>T

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Likely benign
Review star
Show details

Links

DGUOK

Type	Database	ID	Link
Gene	MIM	601465	OMIM
	HGNC	2858	HGNC
	Ensembl	ENSG00000114956	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Likely benign	2023-02-20	criteria provided, single submitter	DGUOK-related disorder	germline	Detail

CIViC

[No Data.]

DisGeNET

[No Data.]

Annotation

Annotations

Descrption	Source	Links
NM_080916.3(DGUOK):c.143-19C>T AND DGUOK-related disorder	ClinVar	Detail

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
Genome: hg38
Position: chr2:73,938,891-73,938,891
Variant Type: snv
Reference Allele: C
Alternative Allele: T

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