chr13:32915083:TG> Detail (hg19) (BRCA2)

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

Genome

Assembly	Position
hg19	chr13:32,915,083-32,915,084
hg38	chr13:32,340,946-32,340,947

HGVS

BRCA2

Type	Transcript	Protein
RefSeq	NM_000059.3:c.6591_6592delTG	NP_000050.2:p.Glu2198AsnfsTer4
Ensemble	ENST00000380152.8:c.6591_6592delTG	ENST00000380152.8:p.Glu2198AsnfsTer4
	ENST00000530893.7:c.6222_6223delTG	ENST00000530893.7:p.Glu2075AsnfsTer4
	ENST00000544455.6:c.6591_6592delTG	ENST00000544455.6:p.Glu2198AsnfsTer4
	ENST00000700202.2:c.6591_6592delTG	ENST00000700202.2:p.Glu2198AsnfsTer4
	ENST00000713678.1:c.6591_6592delTG	ENST00000713678.1:p.Glu2198AsnfsTer4
	ENST00000713680.1:c.6591_6592delTG	ENST00000713680.1:p.Glu2198AsnfsTer4

Summary

MGeND

Clinical significance	Pathogenic
Variant entry	1
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance	Pathogenic
Review star
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Links

BRCA2

Type	Database	ID	Link
Gene	MIM	600185	OMIM
	HGNC	1101	HGNC
	Ensembl	ENSG00000139618	Ensembl
	NCBI		NCBI
	Gene Cards		Gene Cards
	OncoKB		OncoKB

Type	Database	ID	Link
Variant	TogoVar
	COSMIC	COSM6951360	COSMIC
	MONDO

Disease area statistics

MGeND

Clinical significance	Last evaluated	Condition	Origin	Submission ID	Submitter	Institute	Citation	Comment	Image
Pathogenic	2020/04/20	descending colon	not provided	MGS000042 (TMGS000093)	Hitoshi Nakagama	National Cancer Center Japan

ClinVar

Clinical significance	Last evaluated	Review status	Condition	Origin	Links
Pathogenic	2016-09-08	reviewed by expert panel	Breast-ovarian cancer, familial, susceptibility to, 2	germline not provided unknown	Detail
Pathogenic	2023-12-14	criteria provided, multiple submitters, no conflicts	hereditary breast ovarian cancer syndrome	germline unknown	Detail
Pathogenic	2023-02-17	criteria provided, multiple submitters, no conflicts	Hereditary cancer-predisposing syndrome	germline	Detail
Pathogenic	2020-11-11	criteria provided, multiple submitters, no conflicts	not provided	germline unknown	Detail
Pathogenic	2016-03-03	criteria provided, single submitter	Breast and/or ovarian cancer	germline	Detail
Pathogenic	2022-04-01	criteria provided, single submitter	Malignant tumor of prostate	germline	Detail
Pathogenic	2023-02-21	no assertion criteria provided	endometrial carcinoma	germline	Detail
Pathogenic	2023-07-13	criteria provided, single submitter	Familial cancer of breast	unknown	Detail

CIViC

[No Data.]

DisGeNET

Score	Disease name	Description	Source	Pubmed	Links
0.240	Breast-ovarian cancer, familial, susceptibility to, 2	NA	CLINVAR		Detail
0.391	Hereditary Breast and Ovarian Cancer Syndrome	NA	CLINVAR		Detail
0.128	Neoplastic Syndromes, Hereditary	NA	CLINVAR		Detail

Annotation

Annotations

Descrption	Source	Links
NM_000059.4(BRCA2):c.6591_6592del (p.Glu2198fs) AND Breast-ovarian cancer, familial, susceptibility ...	ClinVar	Detail
NM_000059.4(BRCA2):c.6591_6592del (p.Glu2198fs) AND Hereditary breast ovarian cancer syndrome	ClinVar	Detail
NM_000059.4(BRCA2):c.6591_6592del (p.Glu2198fs) AND Hereditary cancer-predisposing syndrome	ClinVar	Detail
NM_000059.4(BRCA2):c.6591_6592del (p.Glu2198fs) AND not provided	ClinVar	Detail
NM_000059.4(BRCA2):c.6591_6592del (p.Glu2198fs) AND Breast and/or ovarian cancer	ClinVar	Detail
NM_000059.4(BRCA2):c.6591_6592del (p.Glu2198fs) AND Malignant tumor of prostate	ClinVar	Detail
NM_000059.4(BRCA2):c.6591_6592del (p.Glu2198fs) AND Endometrial carcinoma	ClinVar	Detail
NM_000059.4(BRCA2):c.6591_6592del (p.Glu2198fs) AND Familial cancer of breast	ClinVar	Detail
NA	DisGeNET	Detail
NA	DisGeNET	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: rs80359605 dbSNP
Genome: hg19
Position: chr13:32,915,083-32,915,084
Variant Type: snv
Reference Allele: TG
Alternative Allele: -

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