chr13:32337521:C>A Detail (hg38) (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	chr13:32,911,658-32,911,658 View the variant detail on this assembly version.
hg38	chr13:32,337,521-32,337,521

HGVS

BRCA2

Type	Transcript	Protein
RefSeq	NM_000059.3:c.3166C>A	NP_000050.2:p.Gln1056Lys
Ensemble	ENST00000380152.8:c.3166C>A	ENST00000380152.8:p.Gln1056Lys
	ENST00000530893.7:c.2797C>A	ENST00000530893.7:p.Gln933Lys
	ENST00000544455.6:c.3166C>A	ENST00000544455.6:p.Gln1056Lys
	ENST00000700202.2:c.3166C>A	ENST00000700202.2:p.Gln1056Lys
	ENST00000713678.1:c.3166C>A	ENST00000713678.1:p.Gln1056Lys
	ENST00000713680.1:c.3166C>A	ENST00000713680.1:p.Gln1056Lys

Summary

MGeND

Clinical significance
Variant entry
GWAS entry
Disease area statistics	Show details

Frequency

[No Data.]

Prediction

ClinVar

Clinical Significance
Review star	[No Data.]
Show details

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
	MONDO

Disease area statistics

[No Data.]

MGeND

[No Data.]

ClinVar

[No Data.]

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

Annotation

Annotations

Descrption	Source	Links
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: rs79728106 dbSNP
Genome: hg38
Position: chr13:32,337,521-32,337,521
Variant Type: snv
Reference Allele: C
Alternative Allele: A

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