chr8:89953366:C>A Detail (hg38) (NBN)

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

Genome

Assembly	Position
hg19	chr8:90,965,594-90,965,594 View the variant detail on this assembly version.
hg38	chr8:89,953,366-89,953,366

HGVS

NBN

Type	Transcript	Protein
RefSeq	NM_002485.4:c.1723G>T	NP_002476.2:p.Glu575Ter
	NM_001024688.2:c.1477G>T	NP_001019859.1:p.Glu493Ter
Ensemble	ENST00000265433.8:c.1723G>T	ENST00000265433.8:p.Glu575Ter
	ENST00000409330.5:c.1477G>T	ENST00000409330.5:p.Glu493Ter
	ENST00000517337.2:c.1477G>T	ENST00000517337.2:p.Glu493Ter
	ENST00000523444.2:c.1477G>T	ENST00000523444.2:p.Glu493Ter
	ENST00000697292.1:c.1723G>T	ENST00000697292.1:p.Glu575Ter
	ENST00000697293.1:c.1723G>T	ENST00000697293.1:p.Glu575Ter
	ENST00000697298.1:c.1477G>T	ENST00000697298.1:p.Glu493Ter
	ENST00000697299.1:c.1477G>T	ENST00000697299.1:p.Glu493Ter
	ENST00000697304.1:c.1411G>T	ENST00000697304.1:p.Glu471Ter
	ENST00000697307.1:c.1723G>T	ENST00000697307.1:p.Glu575Ter
	ENST00000697308.1:c.1723G>T	ENST00000697308.1:p.Glu575Ter
	ENST00000697309.1:c.1723G>T	ENST00000697309.1:p.Glu575Ter
	ENST00000697310.1:c.1723G>T	ENST00000697310.1:p.Glu575Ter

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic Likely pathogenic
Review star
Show details

Links

NBN

Type	Database	ID	Link
Gene	MIM	602667	OMIM
	HGNC	7652	HGNC
	Ensembl	ENSG00000104320	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
Pathogenic	2023-03-16	criteria provided, single submitter	Hereditary cancer-predisposing syndrome	germline	Detail
Pathogenic Likely pathogenic	2023-09-08	criteria provided, multiple submitters, no conflicts	Microcephaly, normal intelligence and immunodeficiency	germline unknown	Detail
Pathogenic	2021-07-21	criteria provided, single submitter	aplastic anemia	unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.120	Neoplastic Syndromes, Hereditary	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_002485.5(NBN):c.1723G>T (p.Glu575Ter) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_002485.5(NBN):c.1723G>T (p.Glu575Ter) AND Microcephaly, normal intelligence and immunodeficiency	ClinVar	Detail
NM_002485.5(NBN):c.1723G>T (p.Glu575Ter) AND Aplastic anemia	ClinVar	Detail
NA	DisGeNET	Detail

Overlapped Transcript Coordinates

Gene	Transcript ID	Exon Number	Chromosome	Start	Stop	Type	Amino Mutation	Transcript Position	Links

Overlapped Transcript

Gene	Transcript ID	Chromosome	Start	Stop	Links

Gene: -
dbSNP: rs786201745 dbSNP
Genome: hg38
Position: chr8:89,953,366-89,953,366
Variant Type: snv
Reference Allele: C
Alternative Allele: A

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