List of variants in gene BRCA2 reported by Equipe Genetique des Anomalies du Developpement, Université de Bourgogne

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.5946del (p.Ser1982fs)	rs80359550	0.00019
NM_000059.4(BRCA2):c.9294C>G (p.Tyr3098Ter)	rs80359200	0.00002
NM_000059.4(BRCA2):c.2612C>A (p.Ser871Ter)	rs397507634	0.00001
NM_000059.4(BRCA2):c.2175dup (p.Val726fs)	rs276174819
NM_000059.4(BRCA2):c.3172A>T (p.Lys1058Ter)	rs730881521
NM_000059.4(BRCA2):c.5616_5620del (p.Lys1872fs)	rs80359525
NM_000059.4(BRCA2):c.8218_8222del (p.Leu2740fs)	rs1566245731
NM_000059.4(BRCA2):c.9294C>A (p.Tyr3098Ter)	rs80359200

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