List of variants in gene BRCA2 reported as likely pathogenic by Genomic Center, National Cancer Institute

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.1508del (p.Lys503fs)	rs886038066
NM_000059.4(BRCA2):c.2514del (p.Lys838fs)	rs886040433
NM_000059.4(BRCA2):c.3440del (p.Asn1147fs)	rs2548525957
NM_000059.4(BRCA2):c.3935del (p.Asn1312fs)	rs1566229411
NM_000059.4(BRCA2):c.3956del (p.Asn1319fs)	rs2137501511
NM_000059.4(BRCA2):c.4468del (p.Ile1490fs)	rs2548528447
NM_000059.4(BRCA2):c.4904del (p.Phe1634_Leu1635insTer)	rs80359471
NM_000059.4(BRCA2):c.4997del (p.Asn1666fs)	rs2548529774
NM_000059.4(BRCA2):c.7340del (p.Asn2447fs)	rs786204281
NM_000059.4(BRCA2):c.7654del (p.Ile2552fs)	rs879255463
NM_000059.4(BRCA2):c.7704del (p.Phe2568fs)	rs2548542582
NM_000059.4(BRCA2):c.937del (p.Ser313fs)	rs2137466022
NM_000059.4(BRCA2):c.9799_9800del (p.Lys3267fs)	rs1566261027
NM_000059.4(BRCA2):c.9981del (p.Lys3327fs)	rs1328254546

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