List of variants in gene BRCA2 reported as pathogenic by Yang An-Suei Laboratory, Academia Sinica

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.3883C>T (p.Gln1295Ter)	rs879255309	0.00001
NM_000059.4(BRCA2):c.-5_11del (p.Met1fs)	rs1555280073
NM_000059.4(BRCA2):c.2095C>T (p.Gln699Ter)	rs878853559
NM_000059.4(BRCA2):c.2754del (p.Asn918fs)	rs1555282830
NM_000059.4(BRCA2):c.2990T>G (p.Leu997Ter)	rs397507649
NM_000059.4(BRCA2):c.3322A>T (p.Lys1108Ter)	rs1555283169
NM_000059.4(BRCA2):c.800dup (p.Thr269fs)	rs1555281594
NM_000059.4(BRCA2):c.8206del (p.Leu2736fs)	rs397507396
NM_000059.4(BRCA2):c.8400_8402delinsAAAA (p.Phe2801fs)	rs483353077
NM_000059.4(BRCA2):c.857C>G (p.Ser286Ter)	rs1131692035

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